Canonical Allele Identifier: CA742240642
Gene:

Linked Data

dbSNP Id: rs1265106805

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23661810C>T , CM000682.2:g.23661810C>T GRCh38
NC_000020.10:g.23642447C>T , CM000682.1:g.23642447C>T GRCh37
NC_000020.9:g.23590447C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001754712.1:n.280+160C>T