Canonical Allele Identifier: CA2749022111
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.17844085T>A , CM000664.2:g.17844085T>A GRCh38
NC_000002.11:g.18025352T>A , CM000664.1:g.18025352T>A GRCh37
NC_000002.10:g.17888833T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939764.2:n.447+3609A>T