Canonical Allele Identifier: CA1258276567
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.67637567A= , CM000664.2:g.67637567A= GRCh38
NC_000002.11:g.67864699A= , CM000664.1:g.67864699A= GRCh37
NC_000002.10:g.67718203A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739524.1:n.65+13399T=