Linked Data
ClinVar Variation Id:
1051615
ClinVar RCV Id:
RCV001359681
dbSNP Id:
rs377467259
gnomAD v2:
3-38793973-G-C
gnomAD v4:
3-38752482-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.38752482G>C , CM000665.2:g.38752482G>C | GRCh38 |
| NC_000003.11:g.38793973G>C , CM000665.1:g.38793973G>C | GRCh37 |
| NC_000003.10:g.38768977G>C | NCBI36 |
| NG_031891.2:g.46529C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000449082.3:c.1492C>G MANE Select | ENSP00000390600.2:p.Arg498Gly | |
| ENST00000643924.1:c.1492C>G | ENSP00000495595.1:p.Arg498Gly | |
| ENST00000655275.1:c.1519C>G | ENSP00000499510.1:p.Arg507Gly | |
| ENST00000449082.2:c.1492C>G | ENSP00000390600.2:p.Arg498Gly | |
| NM_001293306.2:c.1492C>G | NP_001280235.2:p.Arg498Gly | |
| NM_001293307.2:c.1462-2298C>G | NP_001280236.2:n.1462-2298C>G | |
| NM_006514.3:c.1492C>G | NP_006505.3:p.Arg498Gly | |
| XM_005265371.2:c.1501C>G | XP_005265428.1:p.Arg501Gly | |
| XM_011533993.1:c.1501C>G | XP_011532295.1:p.Arg501Gly | |
| XM_011533994.1:c.1471-2298C>G | XP_011532296.1:n.1471-2298C>G | |
| XM_005265371.3:c.1501C>G | XP_005265428.1:p.Arg501Gly | |
| XM_011533993.2:c.1501C>G | XP_011532295.1:p.Arg501Gly | |
| XM_011533994.2:c.1471-2298C>G | XP_011532296.1:n.1471-2298C>G | |
| NM_006514.4:c.1492C>G MANE Select | NP_006505.4:p.Arg498Gly |