Canonical Allele Identifier: CA1968513077
Gene:

Linked Data

dbSNP Id: rs1856778780

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45506623T>A , CM000673.2:g.45506623T>A GRCh38
NC_000011.9:g.45528173T>A , CM000673.1:g.45528173T>A GRCh37
NC_000011.8:g.45484749T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001748204.2:n.909-16852A>T
XR_931245.3:n.566-16852A>T