Linked Data
dbSNP Id:
rs769786931
ExAC:
1:43396466 C / T
gnomAD v2:
1-43396466-C-T
gnomAD v4:
1-42930795-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.42930795C>T , CM000663.2:g.42930795C>T | GRCh38 |
| NC_000001.10:g.43396466C>T , CM000663.1:g.43396466C>T | GRCh37 |
| NC_000001.9:g.43169053C>T | NCBI36 |
| NG_008232.1:g.33382G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000426263.10:c.347G>A MANE Select | ENSP00000416293.2:p.Gly116Asp | |
| ENST00000674765.1:c.347G>A | ENSP00000501811.1:p.Gly116Asp | |
| ENST00000675112.1:n.370G>A | ||
| ENST00000676254.1:n.796G>A | ||
| ENST00000372500.4:c.251G>A | ENSP00000361578.4:p.Gly84Asp | |
| ENST00000426263.7:c.347G>A | ENSP00000416293.2:p.Gly116Asp | |
| ENST00000439722.2:c.226G>A | ENSP00000395521.2:n.226G>A | |
| ENST00000475162.3:c.246G>A | ||
| ENST00000625233.2:n.555G>A | ||
| ENST00000630287.2:c.347G>A | ENSP00000486694.1:p.Gly116Asp | |
| NM_006516.2:c.347G>A | NP_006507.2:p.Gly116Asp | |
| NM_006516.3:c.347G>A | NP_006507.2:p.Gly116Asp | |
| NM_006516.4:c.347G>A MANE Select | NP_006507.2:p.Gly116Asp |