Canonical Allele Identifier: CA1199280377
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.147089027T= , CM000663.2:g.147089027T= GRCh38
NC_000001.10:g.146560574T= , CM000663.1:g.146560574T= GRCh37
NC_000001.9:g.145027198T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000444082.1:n.1845+20835A=