Linked Data
ClinVar Variation Id:
854004
ClinVar RCV Id:
RCV001058944
dbSNP Id:
rs1979817884
gnomAD v4:
20-46725245-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.46725245A>G , CM000682.2:g.46725245A>G | GRCh38 |
| NC_000020.10:g.45353884A>G , CM000682.1:g.45353884A>G | GRCh37 |
| NC_000020.9:g.44787291A>G | NCBI36 |
| NG_016284.1:g.20606A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000359271.4:c.209A>G MANE Select | ENSP00000352216.2:p.Asp70Gly | |
| ENST00000359271.3:c.209A>G | ENSP00000352216.2:p.Asp70Gly | |
| ENST00000611837.1:n.361A>G | ||
| NM_030777.3:c.209A>G | NP_110404.1:p.Asp70Gly | |
| XM_011529060.1:c.272A>G | XP_011527362.1:p.Asp91Gly | |
| XM_011529061.1:c.218A>G | XP_011527363.1:p.Asp73Gly | |
| XM_011529062.1:c.272A>G | XP_011527364.1:p.Asp91Gly | |
| XM_011529063.1:c.272A>G | XP_011527365.1:p.Asp91Gly | |
| XM_011529064.1:c.272A>G | XP_011527366.1:p.Asp91Gly | |
| XM_011529065.1:c.272A>G | XP_011527367.1:p.Asp91Gly | |
| XR_936641.1:n.408A>G | ||
| XM_011529060.2:c.272A>G | XP_011527362.1:p.Asp91Gly | |
| XM_011529061.2:c.218A>G | XP_011527363.1:p.Asp73Gly | |
| XM_011529062.2:c.272A>G | XP_011527364.1:p.Asp91Gly | |
| XM_011529063.2:c.272A>G | XP_011527365.1:p.Asp91Gly | |
| XM_011529064.2:c.272A>G | XP_011527366.1:p.Asp91Gly | |
| XM_011529065.2:c.272A>G | XP_011527367.1:p.Asp91Gly | |
| XM_017028087.2:c.209A>G | XP_016883576.1:p.Asp70Gly | |
| XR_936641.2:n.395A>G | ||
| NM_030777.4:c.209A>G MANE Select | NP_110404.1:p.Asp70Gly |