Linked Data
ClinVar Variation Id:
2159042
ClinVar RCV Id:
RCV003072609
dbSNP Id:
rs149578923
ExAC:
12:116429467 C / T
gnomAD v2:
12-116429467-C-T
gnomAD v3:
12-115991662-C-T
gnomAD v4:
12-115991662-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.115991662C>T , CM000674.2:g.115991662C>T | GRCh38 |
| NC_000012.11:g.116429467C>T , CM000674.1:g.116429467C>T | GRCh37 |
| NC_000012.10:g.114913850C>T | NCBI36 |
| NG_023366.1:g.290525G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000281928.9:c.3292G>A MANE Select | ENSP00000281928.3:p.Ala1098Thr | |
| ENST00000549786.2:c.2720G>A | ||
| ENST00000648379.1:n.1660G>A | ||
| ENST00000648737.1:n.3056G>A | ||
| ENST00000648825.1:n.32G>A | ||
| ENST00000648916.1:n.1303G>A | ||
| ENST00000649607.1:c.1476G>A | ||
| ENST00000650226.1:c.3292G>A | ENSP00000496981.1:p.Ala1098Thr | |
| ENST00000281928.7:c.3292G>A | ENSP00000281928.3:p.Ala1098Thr | |
| NM_015335.4:c.3292G>A | NP_056150.1:p.Ala1098Thr | |
| XM_011538080.1:c.3292G>A | XP_011536382.1:p.Ala1098Thr | |
| XM_011538081.1:c.3289G>A | XP_011536383.1:p.Ala1097Thr | |
| XM_011538082.1:c.3262G>A | XP_011536384.1:p.Ala1088Thr | |
| XM_011538080.2:c.3292G>A | XP_011536382.1:p.Ala1098Thr | |
| XM_011538081.2:c.3289G>A | XP_011536383.1:p.Ala1097Thr | |
| XM_011538082.2:c.3262G>A | XP_011536384.1:p.Ala1088Thr | |
| XM_017019090.1:c.3289G>A | XP_016874579.1:p.Ala1097Thr | |
| NM_015335.5:c.3292G>A MANE Select | NP_056150.1:p.Ala1098Thr |