Canonical Allele Identifier: CA1769514519
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.20734896C= , CM000670.2:g.20734896C= GRCh38
NC_000008.10:g.20592407C= , CM000670.1:g.20592407C= GRCh37
NC_000008.9:g.20636687C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949569.3:n.72-55550C=