Canonical Allele Identifier: CA1735257917
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.112988389A= , CM000669.2:g.112988389A= GRCh38
NC_000007.13:g.112628444A= , CM000669.1:g.112628444A= GRCh37
NC_000007.12:g.112415680A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110162.1:n.77-1725T=