Canonical Allele Identifier:
CA785915601
Gene:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.116928293G>A , CM000666.2:g.116928293G>A | GRCh38 |
| NC_000004.11:g.117849449G>A , CM000666.1:g.117849449G>A | GRCh37 |
| NC_000004.10:g.118068897G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001741796.1:n.668+28C>T | ||
| XR_001741797.1:n.619+28C>T | ||
| XR_001741798.1:n.671+28C>T | ||
| XR_001741800.1:n.671+28C>T |