Canonical Allele Identifier: CA2516355949
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.20735016A>C , CM000670.2:g.20735016A>C GRCh38
NC_000008.10:g.20592527A>C , CM000670.1:g.20592527A>C GRCh37
NC_000008.9:g.20636807A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949569.3:n.72-55430A>C