Linked Data
ClinVar Variation Id:
1681689
ClinVar RCV Id:
RCV002239199
dbSNP Id:
rs2139997870
gnomAD v4:
12-57489487-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57489487G>A , CM000674.2:g.57489487G>A | GRCh38 |
| NC_000012.11:g.57883270G>A , CM000674.1:g.57883270G>A | GRCh37 |
| NC_000012.10:g.56169537G>A | NCBI36 |
| NG_034077.1:g.6535G>A | |
| NG_023205.2:g.4328C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262027.10:c.343G>A MANE Select | ENSP00000262027.5:p.Gly115Ser | |
| ENST00000262027.9:c.343G>A | ENSP00000262027.5:p.Gly115Ser | |
| ENST00000447721.6:n.133-720G>A | ||
| ENST00000537638.6:c.343G>A | ENSP00000446168.2:p.Gly115Ser | |
| ENST00000545888.6:c.343G>A | ENSP00000439307.2:p.Gly115Ser | |
| ENST00000546481.1:n.529G>A | ||
| ENST00000547501.5:c.312G>A | ENSP00000447145.1:p.Leu104= | |
| ENST00000548674.5:n.313G>A | ||
| ENST00000548714.5:n.444G>A | ||
| ENST00000549074.5:c.200+378G>A | ENSP00000447258.1:n.200+378G>A | |
| ENST00000550449.5:n.456G>A | ||
| ENST00000551431.5:c.279+142G>A | ENSP00000446729.1:n.279+142G>A | |
| ENST00000551842.5:n.366G>A | ||
| ENST00000551892.1:c.110-791G>A | ENSP00000450018.1:n.110-791G>A | |
| ENST00000552007.5:c.200+378G>A | ENSP00000448576.1:n.200+378G>A | |
| ENST00000553123.1:n.567G>A | ||
| ENST00000553162.5:n.366G>A | ||
| ENST00000628866.2:c.279+142G>A | ENSP00000486738.1:n.279+142G>A | |
| ENST00000630571.2:c.200+378G>A | ENSP00000485951.1:n.200+378G>A | |
| ENST00000630803.1:c.110-791G>A | ENSP00000486356.1:n.110-791G>A | |
| NM_004990.3:c.343G>A | NP_004981.2:p.Gly115Ser | |
| XM_006719398.2:c.-284G>A | XP_006719461.1:n.-284G>A | |
| XM_011538353.1:c.343G>A | XP_011536655.1:p.Gly115Ser | |
| XM_006719398.4:c.-284G>A | XP_006719461.1:n.-284G>A | |
| XR_001748704.2:n.366G>A | ||
| XR_002957327.1:n.366G>A | ||
| NM_004990.4:c.343G>A MANE Select | NP_004981.2:p.Gly115Ser |