Canonical Allele Identifier: CA1889344546
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8697632G= , CM000672.2:g.8697632G= GRCh38
NC_000010.10:g.8739595G= , CM000672.1:g.8739595G= GRCh37
NC_000010.9:g.8779601G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930641.1:n.33-27831C=