Canonical Allele Identifier: CA2355978705
Gene:

Linked Data

dbSNP Id: rs1980376989

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23661652T>A , CM000682.2:g.23661652T>A GRCh38
NC_000020.10:g.23642289T>A , CM000682.1:g.23642289T>A GRCh37
NC_000020.9:g.23590289T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001754712.1:n.280+2T>A