Linked Data
dbSNP Id:
rs1214436691
gnomAD v2:
10-115805047-G-A
gnomAD v3:
10-114045288-G-A
gnomAD v4:
10-114045288-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.114045288G>A , CM000672.2:g.114045288G>A | GRCh38 |
| NC_000010.10:g.115805047G>A , CM000672.1:g.115805047G>A | GRCh37 |
| NC_000010.9:g.115795037G>A | NCBI36 |
| NG_012187.1:g.6242G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369295.4:c.1156G>A MANE Select | ENSP00000358301.2:p.Ala386Thr | |
| ENST00000369295.3:c.1156G>A | ENSP00000358301.2:p.Ala386Thr | |
| NM_000684.2:c.1156G>A | NP_000675.1:p.Ala386Thr | |
| NM_000684.3:c.1156G>A MANE Select | NP_000675.1:p.Ala386Thr |