Linked Data
ClinVar Variation Id:
1473866
ClinVar RCV Id:
RCV001970908
dbSNP Id:
rs1865821627
gnomAD v4:
12-13866021-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.13866021G>A , CM000674.2:g.13866021G>A | GRCh38 |
| NC_000012.11:g.14018955G>A , CM000674.1:g.14018955G>A | GRCh37 |
| NC_000012.10:g.13910222G>A | NCBI36 |
| NG_031854.1:g.119068C>T | |
| NG_031854.2:g.120992C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000609686.4:c.188C>T MANE Select | ENSP00000477455.1:p.Ser63Phe | |
| ENST00000630791.2:c.188C>T | ENSP00000486677.2:p.Ser63Phe | |
| ENST00000609686.3:c.188C>T | ENSP00000477455.1:p.Ser63Phe | |
| NM_000834.3:c.188C>T | NP_000825.2:p.Ser63Phe | |
| XM_011520628.1:c.188C>T | XP_011518930.1:p.Ser63Phe | |
| XM_011520629.1:c.188C>T | XP_011518931.1:p.Ser63Phe | |
| XM_011520630.1:c.188C>T | XP_011518932.1:p.Ser63Phe | |
| NM_000834.4:c.188C>T | NP_000825.2:p.Ser63Phe | |
| XM_011520628.2:c.188C>T | XP_011518930.1:p.Ser63Phe | |
| XM_011520629.2:c.188C>T | XP_011518931.1:p.Ser63Phe | |
| XM_017019219.2:c.188C>T | XP_016874708.1:p.Ser63Phe | |
| NM_000834.5:c.188C>T MANE Select | NP_000825.2:p.Ser63Phe |