Canonical Allele Identifier: CA2255111872
Gene:

Linked Data

dbSNP Id: rs1597650264

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237185A>G , CM000679.2:g.30237185A>G GRCh38
NC_000017.10:g.28564203A>G , CM000679.1:g.28564203A>G GRCh37
NC_000017.9:g.25588329A>G NCBI36
NG_011747.2:g.3752T>C

Transcript Alleles

HGVS Amino-acid change
XR_934654.1:n.165+115A>G
XR_001752824.1:n.280+115A>G