Canonical Allele Identifier: CA1320446104
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200033096A= , CM000664.2:g.200033096A= GRCh38
NC_000002.11:g.200897819A= , CM000664.1:g.200897819A= GRCh37
NC_000002.10:g.200606064A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923778.1:n.178-22200T=