Canonical Allele Identifier: CA2355978762
Gene:

Linked Data

dbSNP Id: rs1980380510

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23661764G>T , CM000682.2:g.23661764G>T GRCh38
NC_000020.10:g.23642401G>T , CM000682.1:g.23642401G>T GRCh37
NC_000020.9:g.23590401G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001754712.1:n.280+114G>T