Canonical Allele Identifier: CA13689964
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68253933G>A , CM000674.2:g.68253933G>A GRCh38
NC_000012.11:g.68647713G>A , CM000674.1:g.68647713G>A GRCh37
NC_000012.10:g.66933980G>A NCBI36
NG_060763.1:g.4672C>T

Transcript Alleles

HGVS Amino-acid Change
XR_945055.1:n.265-10725G>A
XR_002957418.1:n.281-10725G>A