Canonical Allele Identifier: CA1689217936
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.13400476A= , CM000669.2:g.13400476A= GRCh38
NC_000007.13:g.13440101A= , CM000669.1:g.13440101A= GRCh37
NC_000007.12:g.13406626A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745097.1:n.147+90153A=