Linked Data
dbSNP Id:
rs778526991
ExAC:
5:14871581 C / A
gnomAD v2:
5-14871581-C-A
gnomAD v4:
5-14871472-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.14871472C>A , CM000667.2:g.14871472C>A | GRCh38 |
| NC_000005.9:g.14871581C>A , CM000667.1:g.14871581C>A | GRCh37 |
| NC_000005.8:g.14924581C>A | NCBI36 |
| NG_008273.1:g.5307G>T | |
| NG_008273.2:g.5314G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000284268.8:c.-25G>T MANE Select | ENSP00000284268.6:n.-25G>T | |
| ENST00000284268.6:c.-25G>T | ENSP00000284268.6:n.-25G>T | |
| ENST00000505140.1:c.-25G>T | ENSP00000426332.1:n.-25G>T | |
| ENST00000513115.1:n.1G>T | ||
| NM_054027.4:c.-25G>T | NP_473368.1:n.-25G>T | |
| XM_011514067.1:c.-25G>T | XP_011512369.1:n.-25G>T | |
| NM_054027.5:c.-25G>T | NP_473368.1:n.-25G>T | |
| NM_054027.6:c.-25G>T MANE Select | NP_473368.1:n.-25G>T |