Canonical Allele Identifier: CA1199280385
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.147089046A= , CM000663.2:g.147089046A= GRCh38
NC_000001.10:g.146560593A= , CM000663.1:g.146560593A= GRCh37
NC_000001.9:g.145027217A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000444082.1:n.1845+20816T=