Canonical Allele Identifier: CA313629798
Gene:

Linked Data

dbSNP Id: rs560851460

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23661820C>T , CM000682.2:g.23661820C>T GRCh38
NC_000020.10:g.23642457C>T , CM000682.1:g.23642457C>T GRCh37
NC_000020.9:g.23590457C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001754712.1:n.280+170C>T