Canonical Allele Identifier: CA1300037053
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155400189G>C , CM000664.2:g.155400189G>C GRCh38
NC_000002.11:g.156256701G>C , CM000664.1:g.156256701G>C GRCh37
NC_000002.10:g.155964947G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923496.1:n.47-4077G>C
XR_923496.2:n.223-4077G>C