Canonical Allele Identifier: CA1769514590
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.20735028C= , CM000670.2:g.20735028C= GRCh38
NC_000008.10:g.20592539C= , CM000670.1:g.20592539C= GRCh37
NC_000008.9:g.20636819C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949569.3:n.72-55418C=