Linked Data
ClinVar Variation Id:
2413361
ClinVar RCV Id:
RCV003110364
dbSNP Id:
rs774971648
ExAC:
19:1401321 G / C
gnomAD v2:
19-1401321-G-C
gnomAD v4:
19-1401322-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.1401322G>C , CM000681.2:g.1401322G>C | GRCh38 |
| NC_000019.9:g.1401321G>C , CM000681.1:g.1401321G>C | GRCh37 |
| NC_000019.8:g.1352321G>C | NCBI36 |
| NG_009785.1:g.5232C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252288.8:c.155C>G MANE Select | ENSP00000252288.1:p.Ala52Gly | |
| ENST00000447102.8:c.155C>G | ENSP00000403536.2:p.Ala52Gly | |
| ENST00000640762.1:c.112+43C>G | ENSP00000492031.1:n.112+43C>G | |
| ENST00000252288.6:c.155C>G | ENSP00000252288.1:p.Ala52Gly | |
| ENST00000447102.7:c.155C>G | ENSP00000403536.2:p.Ala52Gly | |
| NM_000156.5:c.155C>G | NP_000147.1:p.Ala52Gly | |
| NM_138924.2:c.155C>G | NP_620279.1:p.Ala52Gly | |
| NM_000156.6:c.155C>G MANE Select | NP_000147.1:p.Ala52Gly | |
| NM_138924.3:c.155C>G | NP_620279.1:p.Ala52Gly |