Canonical Allele Identifier: CA1068370729
Gene:

Linked Data

dbSNP Id: rs1728164618

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134601426A>G , CM000666.2:g.134601426A>G GRCh38
NC_000004.11:g.135522581A>G , CM000666.1:g.135522581A>G GRCh37
NC_000004.10:g.135742031A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939212.1:n.410+14067A>G
XR_939214.1:n.392+14067A>G
XR_939214.2:n.392+14067A>G