Canonical Allele Identifier: CA1769514580
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.20735012C= , CM000670.2:g.20735012C= GRCh38
NC_000008.10:g.20592523C= , CM000670.1:g.20592523C= GRCh37
NC_000008.9:g.20636803C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949569.3:n.72-55434C=