Canonical Allele Identifier: CA32228035
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs10918196

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165478920T>C , CM000663.2:g.165478920T>C GRCh38
NC_000001.10:g.165448157T>C , CM000663.1:g.165448157T>C GRCh37
NC_000001.9:g.163714781T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_026744.2:n.1530-1805A>G