Canonical Allele Identifier:
CA1661827465
Gene:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.126530014C>A , CM000668.2:g.126530014C>A | GRCh38 |
| NC_000006.11:g.126851160C>A , CM000668.1:g.126851160C>A | GRCh37 |
| NC_000006.10:g.126892853C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650727.1:n.3036+1649G>T | ||
| ENST00000651326.1:n.2289+43758G>T | ||
| ENST00000652383.1:n.630+1649G>T | ||
| ENST00000652545.1:n.3346+1649G>T |