Canonical Allele Identifier: CA1320446162
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200033209T= , CM000664.2:g.200033209T= GRCh38
NC_000002.11:g.200897932T= , CM000664.1:g.200897932T= GRCh37
NC_000002.10:g.200606177T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923778.1:n.178-22313A=