Canonical Allele Identifier: CA1573933651
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113660900A= , CM000667.2:g.113660900A= GRCh38
NC_000005.9:g.112996597A= , CM000667.1:g.112996597A= GRCh37
NC_000005.8:g.113024496A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001742841.1:n.59+27536A=