Canonical Allele Identifier: CA1665604347
Gene:

Linked Data

dbSNP Id: rs9321475

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.134773168T>A , CM000668.2:g.134773168T>A GRCh38
NC_000006.11:g.135094306T>A , CM000668.1:g.135094306T>A GRCh37
NC_000006.10:g.135135999T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943008.1:n.368+32570A>T
XR_943009.1:n.368+32570A>T
XR_001744363.1:n.414+32570A>T
XR_001744364.1:n.342+32570A>T