Canonical Allele Identifier: CA2777062305
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.97388606C>A , CM000669.2:g.97388606C>A GRCh38
NC_000007.13:g.97017918C>A , CM000669.1:g.97017918C>A GRCh37
NC_000007.12:g.96855854C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001745293.1:n.127-59959G>T