Canonical Allele Identifier: CA2782088769
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125478336T>C , CM000670.2:g.125478336T>C GRCh38
NC_000008.10:g.126490578T>C , CM000670.1:g.126490578T>C GRCh37
NC_000008.9:g.126559760T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928628.1:n.256+5022T>C