Canonical Allele Identifier: CA2752787479
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870769C>A , CM000664.2:g.155870769C>A GRCh38
NC_000002.11:g.156727281C>A , CM000664.1:g.156727281C>A GRCh37
NC_000002.10:g.156435527C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923501.1:n.320-3582G>T
XR_001739749.1:n.331-29785G>T
XR_001739750.1:n.331-29785G>T
XR_001739751.1:n.331-29785G>T
XR_923501.2:n.331-3582G>T