Canonical Allele Identifier: CA1320446179
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200033236C= , CM000664.2:g.200033236C= GRCh38
NC_000002.11:g.200897959C= , CM000664.1:g.200897959C= GRCh37
NC_000002.10:g.200606204C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923778.1:n.178-22340G=