Canonical Allele Identifier: CA2043864123
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68248070A= , CM000674.2:g.68248070A= GRCh38
NC_000012.11:g.68641850A= , CM000674.1:g.68641850A= GRCh37
NC_000012.10:g.66928117A= NCBI36
NG_060763.1:g.10535T=

Transcript Alleles

HGVS Amino-acid change
XR_945055.1:n.265-16588A=
XR_002957418.1:n.281-16588A=