Canonical Allele Identifier: CA2002576340
Gene:

Linked Data

dbSNP Id: rs1861335138

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116442681G>A , CM000673.2:g.116442681G>A GRCh38
NC_000011.9:g.116313398G>A , CM000673.1:g.116313398G>A GRCh37
NC_000011.8:g.115818608G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001748403.1:n.349+31196C>T