Canonical Allele Identifier: CA1104780586
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.97388349C>A , CM000669.2:g.97388349C>A GRCh38
NC_000007.13:g.97017661C>A , CM000669.1:g.97017661C>A GRCh37
NC_000007.12:g.96855597C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745293.1:n.127-59702G>T