Linked Data
ClinVar Variation Id:
1588841
ClinVar RCV Id:
RCV002098515
dbSNP Id:
rs994716085
gnomAD v2:
1-154543974-G-A
gnomAD v4:
1-154571498-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.154571498G>A , CM000663.2:g.154571498G>A | GRCh38 |
| NC_000001.10:g.154543974G>A , CM000663.1:g.154543974G>A | GRCh37 |
| NC_000001.9:g.152810598G>A | NCBI36 |
| NG_008027.1:g.8718G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368476.4:c.675G>A MANE Select | ENSP00000357461.3:p.Thr225= | |
| ENST00000636034.1:c.675G>A | ENSP00000489703.1:p.Thr225= | |
| ENST00000637900.1:c.681G>A | ENSP00000490474.1:p.Thr227= | |
| ENST00000368476.3:c.675G>A | ENSP00000357461.3:p.Thr225= | |
| NM_000748.2:c.675G>A | NP_000739.1:p.Thr225= | |
| XM_017000180.2:c.165G>A | XP_016855669.1:p.Thr55= | |
| XR_001736952.2:n.927G>A | ||
| NM_000748.3:c.675G>A MANE Select | NP_000739.1:p.Thr225= |