Canonical Allele Identifier: CA291560818
Gene:

Linked Data

dbSNP Id: rs886296691

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50211713C>T , CM000679.2:g.50211713C>T GRCh38
NC_000017.10:g.48289074C>T , CM000679.1:g.48289074C>T GRCh37
NC_000017.9:g.45644073C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934838.1:n.43-2122C>T