Canonical Allele Identifier: CA15702964
Gene:

Linked Data

dbSNP Id: rs1488665

Genomic Alleles

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

Transcript Alleles

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