Canonical Allele Identifier: CA807669880
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.172771552G>C , CM000667.2:g.172771552G>C GRCh38
NC_000005.9:g.172198555G>C , CM000667.1:g.172198555G>C GRCh37
NC_000005.8:g.172131161G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_941232.1:n.144G>C
XR_941233.1:n.144G>C