Canonical Allele Identifier: CA2500758813
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.67637615C>A , CM000664.2:g.67637615C>A GRCh38
NC_000002.11:g.67864747C>A , CM000664.1:g.67864747C>A GRCh37
NC_000002.10:g.67718251C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739524.1:n.65+13351G>T