Canonical Allele Identifier: CA289293304
Gene:

Linked Data

dbSNP Id: rs1026845359

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237200A>G , CM000679.2:g.30237200A>G GRCh38
NC_000017.10:g.28564218A>G , CM000679.1:g.28564218A>G GRCh37
NC_000017.9:g.25588344A>G NCBI36
NG_011747.2:g.3737T>C

Transcript Alleles

HGVS Amino-acid change
XR_934654.1:n.165+130A>G
XR_001752824.1:n.280+130A>G