Canonical Allele Identifier: CA1223909921
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.224068626C= , CM000663.2:g.224068626C= GRCh38
NC_000001.10:g.224256328C= , CM000663.1:g.224256328C= GRCh37
NC_000001.9:g.222322951C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949173.1:n.385+972C=
XR_001737824.1:n.242+972C=