Canonical Allele Identifier: CA634913689
Gene:

Linked Data

dbSNP Id: rs1460041688

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23661817A>G , CM000682.2:g.23661817A>G GRCh38
NC_000020.10:g.23642454A>G , CM000682.1:g.23642454A>G GRCh37
NC_000020.9:g.23590454A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001754712.1:n.280+167A>G