Canonical Allele Identifier: CA1769514533
Gene:

Linked Data

dbSNP Id: rs1799796089

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.20734924G>T , CM000670.2:g.20734924G>T GRCh38
NC_000008.10:g.20592435G>T , CM000670.1:g.20592435G>T GRCh37
NC_000008.9:g.20636715G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949569.3:n.72-55522G>T