Canonical Allele Identifier: CA1968513023
Gene:

Linked Data

dbSNP Id: rs1488665

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45506566T>C , CM000673.2:g.45506566T>C GRCh38
NC_000011.9:g.45528116T>C , CM000673.1:g.45528116T>C GRCh37
NC_000011.8:g.45484692T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001748204.2:n.909-16795A>G
XR_931245.3:n.566-16795A>G