Canonical Allele Identifier: CA2355978812
Gene:

Linked Data

dbSNP Id: rs1980383237

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23661874A>G , CM000682.2:g.23661874A>G GRCh38
NC_000020.10:g.23642511A>G , CM000682.1:g.23642511A>G GRCh37
NC_000020.9:g.23590511A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001754712.1:n.280+224A>G