Canonical Allele Identifier: CA1985859948
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.80851701A= , CM000673.2:g.80851701A= GRCh38
NC_000011.9:g.80562744A= , CM000673.1:g.80562744A= GRCh37
NC_000011.8:g.80240392A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_247272.2:n.124+60590T=