Linked Data
ClinVar Variation Id:
2438816
ClinVar RCV Id:
RCV003139568
dbSNP Id:
rs774716484
ExAC:
17:7126004 G / C
gnomAD v2:
17-7126004-G-C
gnomAD v4:
17-7222685-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7222685G>C , CM000679.2:g.7222685G>C | GRCh38 |
| NC_000017.10:g.7126004G>C , CM000679.1:g.7126004G>C | GRCh37 |
| NC_000017.9:g.7066728G>C | NCBI36 |
| NG_007975.1:g.7852G>C | |
| NG_008391.2:g.2366C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356839.10:c.897G>C MANE Select | ENSP00000349297.5:p.Lys299Asn | |
| ENST00000322910.9:c.*852G>C | ENSP00000325395.5:n.*852G>C | |
| ENST00000350303.9:c.831G>C | ENSP00000344152.5:p.Lys277Asn | |
| ENST00000356839.9:c.897G>C | ENSP00000349297.5:p.Lys299Asn | |
| ENST00000543245.6:c.966G>C | ENSP00000438689.2:p.Lys322Asn | |
| ENST00000578824.5:n.46G>C | ||
| ENST00000581378.5:c.615G>C | ||
| ENST00000582379.1:n.281G>C | ||
| NM_000018.3:c.897G>C | NP_000009.1:p.Lys299Asn | |
| NM_001033859.2:c.831G>C | NP_001029031.1:p.Lys277Asn | |
| NM_001270447.1:c.966G>C | NP_001257376.1:p.Lys322Asn | |
| NM_001270448.1:c.669G>C | NP_001257377.1:p.Lys223Asn | |
| XM_006721516.2:c.897G>C | XP_006721579.2:p.Lys299Asn | |
| XM_011523829.1:c.897G>C | XP_011522131.1:p.Lys299Asn | |
| XM_011523830.1:c.897G>C | XP_011522132.1:p.Lys299Asn | |
| XR_934021.1:n.1004G>C | ||
| XR_934022.1:n.1004G>C | ||
| XR_934023.1:n.1004G>C | ||
| XM_006721516.3:c.897G>C | XP_006721579.2:p.Lys299Asn | |
| XM_011523829.2:c.897G>C | XP_011522131.1:p.Lys299Asn | |
| XM_011523830.2:c.897G>C | XP_011522132.1:p.Lys299Asn | |
| XM_024450741.1:c.897G>C | XP_024306509.1:p.Lys299Asn | |
| XR_934021.2:n.956G>C | ||
| XR_934022.2:n.956G>C | ||
| XR_934023.2:n.956G>C | ||
| NM_000018.4:c.897G>C MANE Select | NP_000009.1:p.Lys299Asn | |
| NM_001033859.3:c.831G>C | NP_001029031.1:p.Lys277Asn | |
| NM_001270447.2:c.966G>C | NP_001257376.1:p.Lys322Asn | |
| NM_001270448.2:c.669G>C | NP_001257377.1:p.Lys223Asn |