Canonical Allele Identifier: CA1963532659
Gene:

Linked Data

dbSNP Id: rs2732552

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.35063045T>A , CM000673.2:g.35063045T>A GRCh38
NC_000011.9:g.35084592T>A , CM000673.1:g.35084592T>A GRCh37
NC_000011.8:g.35041168T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_931192.1:n.768+2075A>T
XR_001748179.1:n.934+2075A>T
XR_001748180.1:n.937+2075A>T
XR_001748181.1:n.2525A>T
XR_001748182.1:n.235+2075A>T
XR_001748183.2:n.1876A>T
XR_931192.2:n.937+2075A>T