Canonical Allele Identifier: CA144313429
Gene:

Linked Data

dbSNP Id: rs1052068334

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98048016A>G , CM000668.2:g.98048016A>G GRCh38
NC_000006.11:g.98495892A>G , CM000668.1:g.98495892A>G GRCh37
NC_000006.10:g.98602613A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.372-51170A>G
XR_942809.1:n.372-51170A>G