Canonical Allele Identifier: CA15634965
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs17724534

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102845764C>T , CM000672.2:g.102845764C>T GRCh38
NC_000010.10:g.104605521C>T , CM000672.1:g.104605521C>T GRCh37
NC_000010.9:g.104595511C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000426243.2:n.170C>T