Linked Data
ClinVar Variation Id:
971376
dbSNP Id:
rs370059118
ExAC:
19:13007817 G / A
gnomAD v2:
19-13007817-G-A
gnomAD v3:
19-12897003-G-A
gnomAD v4:
19-12897003-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.12897003G>A , CM000681.2:g.12897003G>A | GRCh38 |
| NC_000019.9:g.13007817G>A , CM000681.1:g.13007817G>A | GRCh37 |
| NC_000019.8:g.12868817G>A | NCBI36 |
| NG_009292.1:g.10844G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222214.10:c.946G>A MANE Select | ENSP00000222214.4:p.Ala316Thr | |
| ENST00000222214.9:c.946G>A | ENSP00000222214.4:p.Ala316Thr | |
| ENST00000421816.6:n.924G>A | ||
| ENST00000585420.5:n.1276G>A | ||
| ENST00000590530.5:c.*386G>A | ENSP00000468452.1:n.*386G>A | |
| ENST00000591043.1:n.982G>A | ||
| ENST00000591470.5:c.946G>A | ENSP00000466845.1:p.Ala316Thr | |
| NM_000159.3:c.946G>A | NP_000150.1:p.Ala316Thr | |
| NM_013976.3:c.946G>A | NP_039663.1:p.Ala316Thr | |
| NR_102316.1:n.1109G>A | ||
| NR_102317.1:n.1327G>A | ||
| XM_006722721.2:c.946G>A | XP_006722784.1:p.Ala316Thr | |
| XM_011527899.1:c.946G>A | XP_011526201.1:p.Ala316Thr | |
| XM_011527900.1:c.946G>A | XP_011526202.1:p.Ala316Thr | |
| XM_011527899.2:c.946G>A | XP_011526201.1:p.Ala316Thr | |
| XM_011527900.2:c.946G>A | XP_011526202.1:p.Ala316Thr | |
| XM_017026580.1:c.946G>A | XP_016882069.1:p.Ala316Thr | |
| NM_000159.4:c.946G>A MANE Select | NP_000150.1:p.Ala316Thr | |
| NM_013976.4:c.946G>A | NP_039663.1:p.Ala316Thr | |
| NM_013976.5:c.946G>A | NP_039663.1:p.Ala316Thr |