Canonical Allele Identifier: CA1968512902
Gene:

Linked Data

dbSNP Id: rs1856777486

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45506489T>C , CM000673.2:g.45506489T>C GRCh38
NC_000011.9:g.45528039T>C , CM000673.1:g.45528039T>C GRCh37
NC_000011.8:g.45484615T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001748204.2:n.909-16718A>G
XR_931245.3:n.566-16718A>G