Canonical Allele Identifier: CA2505008332
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.211379703G>A , CM000663.2:g.211379703G>A GRCh38
NC_000001.10:g.211553045G>A , CM000663.1:g.211553045G>A GRCh37
NC_000001.9:g.209619668G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001738446.1:n.291+2492C>T