Canonical Allele Identifier: CA1968513065
Gene:

Linked Data

dbSNP Id: rs1856778702

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45506605T>C , CM000673.2:g.45506605T>C GRCh38
NC_000011.9:g.45528155T>C , CM000673.1:g.45528155T>C GRCh37
NC_000011.8:g.45484731T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001748204.2:n.909-16834A>G
XR_931245.3:n.566-16834A>G