Linked Data
dbSNP Id:
rs777117772
ExAC:
19:45296786 C / A
gnomAD v2:
19-45296786-C-A
gnomAD v4:
19-44793529-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.44793529C>A , CM000681.2:g.44793529C>A | GRCh38 |
| NC_000019.9:g.45296786C>A , CM000681.1:g.45296786C>A | GRCh37 |
| NC_000019.8:g.49988626C>A | NCBI36 |
| NG_054718.1:g.20675C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647358.2:c.1193C>A MANE Select | ENSP00000494162.1:p.Ala398Asp | |
| ENST00000270279.7:c.1193C>A | ENSP00000270279.3:p.Ala398Asp | |
| ENST00000341505.4:c.1055C>A | ENSP00000340250.4:p.Ala352Asp | |
| NM_001130852.1:c.1055C>A | NP_001124324.1:p.Ala352Asp | |
| NM_012116.3:c.1193C>A | NP_036248.3:p.Ala398Asp | |
| XM_005258696.2:c.1193C>A | XP_005258753.1:p.Ala398Asp | |
| XM_011526688.1:c.1193C>A | XP_011524990.1:p.Ala398Asp | |
| XM_011526689.1:c.1055C>A | XP_011524991.1:p.Ala352Asp | |
| XR_935783.1:n.1140C>A | ||
| NM_012116.4:c.1193C>A MANE Select | NP_036248.3:p.Ala398Asp | |
| XM_005258696.3:c.1193C>A | XP_005258753.1:p.Ala398Asp | |
| XM_011526688.2:c.1193C>A | XP_011524990.1:p.Ala398Asp | |
| XM_011526689.2:c.1055C>A | XP_011524991.1:p.Ala352Asp | |
| XR_935783.2:n.1145C>A |