Canonical Allele Identifier: CA634913686
Gene:

Linked Data

dbSNP Id: rs1374342895

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23661811C>T , CM000682.2:g.23661811C>T GRCh38
NC_000020.10:g.23642448C>T , CM000682.1:g.23642448C>T GRCh37
NC_000020.9:g.23590448C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001754712.1:n.280+161C>T