Canonical Allele Identifier: CA2002576379
Gene:

Linked Data

dbSNP Id: rs1861335804

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116442779C>T , CM000673.2:g.116442779C>T GRCh38
NC_000011.9:g.116313496C>T , CM000673.1:g.116313496C>T GRCh37
NC_000011.8:g.115818706C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001748403.1:n.349+31098G>A