Linked Data
dbSNP Id:
rs201342763
ExAC:
3:180377358 T / G
gnomAD v3:
3-180659570-T-G
gnomAD v4:
3-180659570-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.180659570T>G , CM000665.2:g.180659570T>G | GRCh38 |
| NC_000003.11:g.180377358T>G , CM000665.1:g.180377358T>G | GRCh37 |
| NC_000003.10:g.181860052T>G | NCBI36 |
| NG_029581.1:g.24926A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000476379.6:c.620A>C MANE Select | ENSP00000417960.2:p.Asp207Ala | |
| ENST00000650641.1:n.699A>C | ||
| ENST00000650889.1:n.792A>C | ||
| ENST00000651046.1:c.620A>C | ENSP00000499175.1:p.Asp207Ala | |
| ENST00000651818.1:n.762A>C | ||
| ENST00000652024.1:n.711A>C | ||
| ENST00000652408.1:n.757A>C | ||
| ENST00000442201.6:c.620A>C | ENSP00000405708.2:p.Asp207Ala | |
| ENST00000476379.5:c.620A>C | ENSP00000417960.1:p.Asp207Ala | |
| NM_181426.1:c.620A>C | NP_852091.1:p.Asp207Ala | |
| NM_181426.2:c.620A>C MANE Select | NP_852091.1:p.Asp207Ala |