Canonical Allele Identifier: CA787553443
Gene:

Linked Data

dbSNP Id: rs1248396260

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134601537A>G , CM000666.2:g.134601537A>G GRCh38
NC_000004.11:g.135522692A>G , CM000666.1:g.135522692A>G GRCh37
NC_000004.10:g.135742142A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939212.1:n.410+14178A>G
XR_939214.1:n.392+14178A>G
XR_939214.2:n.392+14178A>G