Linked Data
ClinVar Variation Id:
489125
dbSNP Id:
rs934287314
gnomAD v2:
10-13151249-C-T
gnomAD v3:
10-13109249-C-T
gnomAD v4:
10-13109249-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.13109249C>T , CM000672.2:g.13109249C>T | GRCh38 |
| NC_000010.10:g.13151249C>T , CM000672.1:g.13151249C>T | GRCh37 |
| NC_000010.9:g.13191255C>T | NCBI36 |
| NG_012876.1:g.14168C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378747.8:c.127C>T MANE Select | ENSP00000368021.3:p.Gln43Ter | |
| ENST00000263036.9:c.127C>T | ENSP00000263036.3:p.Gln43Ter | |
| ENST00000378747.7:c.127C>T | ENSP00000368021.3:p.Gln43Ter | |
| ENST00000378748.7:c.127C>T | ENSP00000368022.3:p.Gln43Ter | |
| ENST00000378752.7:c.127C>T | ENSP00000368027.3:p.Gln43Ter | |
| ENST00000378757.6:c.127C>T | ENSP00000368032.2:p.Gln43Ter | |
| ENST00000378764.6:c.127C>T | ENSP00000368040.1:p.Gln43Ter | |
| ENST00000430081.5:c.127C>T | ENSP00000414747.2:p.Gln43Ter | |
| ENST00000482140.5:c.127C>T | ENSP00000484961.1:p.Gln43Ter | |
| ENST00000487935.1:n.282C>T | ||
| NM_001008211.1:c.127C>T | NP_001008212.1:p.Gln43Ter | |
| NM_001008212.1:c.127C>T | NP_001008213.1:p.Gln43Ter | |
| NM_001008213.1:c.127C>T | NP_001008214.1:p.Gln43Ter | |
| NM_021980.4:c.127C>T | NP_068815.2:p.Gln43Ter | |
| XM_005252336.2:c.127C>T | XP_005252393.2:p.Gln43Ter | |
| XM_005252337.3:c.127C>T | XP_005252394.2:p.Gln43Ter | |
| XM_005252338.2:c.-139C>T | XP_005252395.2:n.-139C>T | |
| NM_001008212.2:c.127C>T MANE Select | NP_001008213.1:p.Gln43Ter |