Canonical Allele Identifier: CA2255111886
Gene:

Linked Data

dbSNP Id: rs1462627232

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237205T>A , CM000679.2:g.30237205T>A GRCh38
NC_000017.10:g.28564223T>A , CM000679.1:g.28564223T>A GRCh37
NC_000017.9:g.25588349T>A NCBI36
NG_011747.2:g.3732A>T

Transcript Alleles

HGVS Amino-acid change
XR_934654.1:n.165+135T>A
XR_001752824.1:n.280+135T>A