Canonical Allele Identifier: CA265579779
Gene:

Linked Data

dbSNP Id: rs1008047777

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.92307326T>C , CM000676.2:g.92307326T>C GRCh38
NC_000014.8:g.92773670T>C , CM000676.1:g.92773670T>C GRCh37
NC_000014.7:g.91843423T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944153.1:n.131+2782T>C