Linked Data
ClinVar Variation Id:
2107902
ClinVar RCV Id:
RCV003033877
dbSNP Id:
rs1449616485
gnomAD v2:
17-40695927-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42543909G>A , CM000679.2:g.42543909G>A | GRCh38 |
| NC_000017.10:g.40695927G>A , CM000679.1:g.40695927G>A | GRCh37 |
| NC_000017.9:g.37949453G>A | NCBI36 |
| NG_011552.1:g.12977G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000225927.7:c.1903G>A MANE Select | ENSP00000225927.1:p.Ala635Thr | |
| ENST00000225927.6:c.1903G>A | ENSP00000225927.1:p.Ala635Thr | |
| ENST00000591587.1:c.1241G>A | ENSP00000467836.1:n.1241G>A | |
| NM_000263.3:c.1903G>A | NP_000254.2:p.Ala635Thr | |
| XM_006721920.2:c.1072G>A | XP_006721983.1:p.Ala358Thr | |
| XM_011524840.1:c.904G>A | XP_011523142.1:p.Ala302Thr | |
| XM_017024687.1:c.1072G>A | XP_016880176.1:p.Ala358Thr | |
| XM_024450771.1:c.1960G>A | XP_024306539.1:p.Ala654Thr | |
| XM_024450772.1:c.904G>A | XP_024306540.1:p.Ala302Thr | |
| NM_000263.4:c.1903G>A MANE Select | NP_000254.2:p.Ala635Thr |