Canonical Allele Identifier: CA2355978795
Gene:

Linked Data

dbSNP Id: rs1980382324

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23661846G>T , CM000682.2:g.23661846G>T GRCh38
NC_000020.10:g.23642483G>T , CM000682.1:g.23642483G>T GRCh37
NC_000020.9:g.23590483G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001754712.1:n.280+196G>T