Linked Data
ClinVar Variation Id:
2896121
ClinVar RCV Id:
RCV003601031
dbSNP Id:
rs2142978323
MyVariant Identifiers:
chr17:g.7125619C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7222300C>G , CM000679.2:g.7222300C>G | GRCh38 |
| NC_000017.10:g.7125619C>G , CM000679.1:g.7125619C>G | GRCh37 |
| NC_000017.9:g.7066343C>G | NCBI36 |
| NG_007975.1:g.7467C>G | |
| NG_008391.2:g.2751G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356839.10:c.876C>G MANE Select | ENSP00000349297.5:p.Thr292= | |
| ENST00000322910.9:c.*831C>G | ENSP00000325395.5:n.*831C>G | |
| ENST00000350303.9:c.810C>G | ENSP00000344152.5:p.Thr270= | |
| ENST00000356839.9:c.876C>G | ENSP00000349297.5:p.Thr292= | |
| ENST00000543245.6:c.945C>G | ENSP00000438689.2:p.Thr315= | |
| ENST00000577191.5:n.1048C>G | ||
| ENST00000581378.5:c.594C>G | ||
| ENST00000582379.1:n.260C>G | ||
| NM_000018.3:c.876C>G | NP_000009.1:p.Thr292= | |
| NM_001033859.2:c.810C>G | NP_001029031.1:p.Thr270= | |
| NM_001270447.1:c.945C>G | NP_001257376.1:p.Thr315= | |
| NM_001270448.1:c.648C>G | NP_001257377.1:p.Thr216= | |
| XM_006721516.2:c.876C>G | XP_006721579.2:p.Thr292= | |
| XM_011523829.1:c.876C>G | XP_011522131.1:p.Thr292= | |
| XM_011523830.1:c.876C>G | XP_011522132.1:p.Thr292= | |
| XR_934021.1:n.983C>G | ||
| XR_934022.1:n.983C>G | ||
| XR_934023.1:n.983C>G | ||
| XM_006721516.3:c.876C>G | XP_006721579.2:p.Thr292= | |
| XM_011523829.2:c.876C>G | XP_011522131.1:p.Thr292= | |
| XM_011523830.2:c.876C>G | XP_011522132.1:p.Thr292= | |
| XM_024450741.1:c.876C>G | XP_024306509.1:p.Thr292= | |
| XR_934021.2:n.935C>G | ||
| XR_934022.2:n.935C>G | ||
| XR_934023.2:n.935C>G | ||
| NM_000018.4:c.876C>G MANE Select | NP_000009.1:p.Thr292= | |
| NM_001033859.3:c.810C>G | NP_001029031.1:p.Thr270= | |
| NM_001270447.2:c.945C>G | NP_001257376.1:p.Thr315= | |
| NM_001270448.2:c.648C>G | NP_001257377.1:p.Thr216= |