Canonical Allele Identifier: CA2713612100
Gene:

Linked Data

dbSNP Id: rs2114807772

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.163765639C>T , CM000668.2:g.163765639C>T GRCh38
NC_000006.11:g.164186671C>T , CM000668.1:g.164186671C>T GRCh37
NC_000006.10:g.164106661C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001744452.1:n.410+6210C>T
XR_001744454.1:n.369+6251C>T
XR_001744455.1:n.346+6274C>T