Canonical Allele Identifier: CA1320446134
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200033145C= , CM000664.2:g.200033145C= GRCh38
NC_000002.11:g.200897868C= , CM000664.1:g.200897868C= GRCh37
NC_000002.10:g.200606113C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923778.1:n.178-22249G=