Canonical Allele Identifier: CA1689218088
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.13400571A= , CM000669.2:g.13400571A= GRCh38
NC_000007.13:g.13440196A= , CM000669.1:g.13440196A= GRCh37
NC_000007.12:g.13406721A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001745097.1:n.147+90248A=