Canonical Allele Identifier: CA2713116947
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812936C>A , CM000668.2:g.155812936C>A GRCh38
NC_000006.11:g.156134070C>A , CM000668.1:g.156134070C>A GRCh37
NC_000006.10:g.156175762C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+19517C>A
XR_943146.1:n.645-897G>T
XR_001744423.1:n.699-897G>T
XR_001744424.1:n.79+19517C>A