Canonical Allele Identifier: CA1140251016
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.147089017G= , CM000663.2:g.147089017G= GRCh38
NC_000001.10:g.146560564G= , CM000663.1:g.146560564G= GRCh37
NC_000001.9:g.145027188G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000444082.1:n.1845+20845C=