Linked Data
dbSNP Id:
rs547472686
gnomAD v2:
19-45412226-G-A
gnomAD v3:
19-44908969-G-A
gnomAD v4:
19-44908969-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.44908969G>A , CM000681.2:g.44908969G>A | GRCh38 |
| NC_000019.9:g.45412226G>A , CM000681.1:g.45412226G>A | GRCh37 |
| NC_000019.8:g.50104066G>A | NCBI36 |
| NG_007084.2:g.8188G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000252486.9:c.673G>A MANE Select | ENSP00000252486.3:p.Ala225Thr | |
| ENST00000252486.8:c.673G>A | ENSP00000252486.3:p.Ala225Thr | |
| ENST00000434152.5:c.751G>A | ENSP00000413653.2:p.Ala251Thr | |
| NM_000041.3:c.673G>A | NP_000032.1:p.Ala225Thr | |
| NM_001302688.1:c.751G>A | NP_001289617.1:p.Ala251Thr | |
| NM_001302689.1:c.673G>A | NP_001289618.1:p.Ala225Thr | |
| NM_001302690.1:c.673G>A | NP_001289619.1:p.Ala225Thr | |
| NM_001302691.1:c.673G>A | NP_001289620.1:p.Ala225Thr | |
| NM_000041.4:c.673G>A MANE Select | NP_000032.1:p.Ala225Thr | |
| NM_001302688.2:c.751G>A | NP_001289617.1:p.Ala251Thr | |
| NM_001302689.2:c.673G>A | NP_001289618.1:p.Ala225Thr | |
| NM_001302691.2:c.673G>A | NP_001289620.1:p.Ala225Thr | |
| NM_001302690.2:c.673G>A | NP_001289619.1:p.Ala225Thr |