Canonical Allele Identifier: CA1223909865
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.224068458C= , CM000663.2:g.224068458C= GRCh38
NC_000001.10:g.224256160C= , CM000663.1:g.224256160C= GRCh37
NC_000001.9:g.222322783C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949173.1:n.385+804C=
XR_001737824.1:n.242+804C=