Canonical Allele Identifier: CA2729743232
Gene:

Linked Data

dbSNP Id: rs2140087082

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52417552C>T , CM000676.2:g.52417552C>T GRCh38
NC_000014.8:g.52884270C>T , CM000676.1:g.52884270C>T GRCh37
NC_000014.7:g.51954020C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943866.1:n.3151G>A