Canonical Allele Identifier: CA13894878
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs6563695

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.39329106G>T , CM000675.2:g.39329106G>T GRCh38
NC_000013.10:g.39903243G>T , CM000675.1:g.39903243G>T GRCh37
NC_000013.9:g.38801243G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001749845.1:n.1449+7165C>A