Linked Data
ClinVar Variation Id:
886296
dbSNP Id:
rs373106880
ExAC:
16:1634268 C / T
gnomAD v2:
16-1634268-C-T
gnomAD v3:
16-1584267-C-T
gnomAD v4:
16-1584267-C-T
COSMIC:
COSM3387246
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.1584267C>T , CM000678.2:g.1584267C>T | GRCh38 |
| NC_000016.9:g.1634268C>T , CM000678.1:g.1634268C>T | GRCh37 |
| NC_000016.8:g.1574269C>T | NCBI36 |
| NG_032783.1:g.32842G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000426508.7:c.1309G>A MANE Select | ENSP00000406012.2:p.Ala437Thr | |
| ENST00000397417.6:c.482G>A | ENSP00000380562.2:p.Arg161His | |
| ENST00000426508.6:c.1309G>A | ENSP00000406012.2:p.Ala437Thr | |
| ENST00000439987.6:n.1370G>A | ||
| NM_014714.3:c.1309G>A | NP_055529.2:p.Ala437Thr | |
| XM_005255725.3:c.1309G>A | XP_005255782.1:p.Ala437Thr | |
| XM_005255726.2:c.1309G>A | XP_005255783.1:p.Ala437Thr | |
| XM_006720989.2:c.1309G>A | XP_006721052.1:p.Ala437Thr | |
| XM_006720990.2:c.1309G>A | XP_006721053.1:p.Ala437Thr | |
| XM_006720991.2:c.1309G>A | XP_006721054.1:p.Ala437Thr | |
| XM_011522766.1:c.1309G>A | XP_011521068.1:p.Ala437Thr | |
| XM_011522767.1:c.334G>A | XP_011521069.1:p.Ala112Thr | |
| XM_011522768.1:c.1309G>A | XP_011521070.1:p.Ala437Thr | |
| XM_011522769.1:c.1309G>A | XP_011521071.1:p.Ala437Thr | |
| XM_011522771.1:c.1309G>A | XP_011521073.1:p.Ala437Thr | |
| XM_011522772.1:c.1309G>A | XP_011521074.1:p.Ala437Thr | |
| NR_135176.1:n.59+3682C>T | ||
| XM_005255725.5:c.1309G>A | XP_005255782.1:p.Ala437Thr | |
| XM_005255726.4:c.1309G>A | XP_005255783.1:p.Ala437Thr | |
| XM_006720990.3:c.1309G>A | XP_006721053.1:p.Ala437Thr | |
| XM_006720991.3:c.1309G>A | XP_006721054.1:p.Ala437Thr | |
| XM_011522766.3:c.1309G>A | XP_011521068.1:p.Ala437Thr | |
| XM_011522767.2:c.334G>A | XP_011521069.1:p.Ala112Thr | |
| XM_011522769.3:c.1309G>A | XP_011521071.1:p.Ala437Thr | |
| XM_011522771.3:c.1309G>A | XP_011521073.1:p.Ala437Thr | |
| XM_011522772.3:c.1309G>A | XP_011521074.1:p.Ala437Thr | |
| XM_017023910.1:c.1309G>A | XP_016879399.1:p.Ala437Thr | |
| XM_017023911.1:c.-389G>A | XP_016879400.1:n.-389G>A | |
| NM_014714.4:c.1309G>A MANE Select | NP_055529.2:p.Ala437Thr |