Canonical Allele Identifier: CA1769514540
Gene:

Linked Data

dbSNP Id: rs1799796187

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.20734934T>C , CM000670.2:g.20734934T>C GRCh38
NC_000008.10:g.20592445T>C , CM000670.1:g.20592445T>C GRCh37
NC_000008.9:g.20636725T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949569.3:n.72-55512T>C