Canonical Allele Identifier: CA2246165710
Gene:

Linked Data

dbSNP Id: rs1981889527

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8137353A>T , CM000679.2:g.8137353A>T GRCh38
NC_000017.10:g.8040671A>T , CM000679.1:g.8040671A>T GRCh37
NC_000017.9:g.7981396A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934202.1:n.183-1496A>T
XR_934203.1:n.70-2124A>T
XR_934202.2:n.414-1496A>T