Canonical Allele Identifier: CA1496030182
Gene:

Linked Data

dbSNP Id: rs1728166379

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134601595T>G , CM000666.2:g.134601595T>G GRCh38
NC_000004.11:g.135522750T>G , CM000666.1:g.135522750T>G GRCh37
NC_000004.10:g.135742200T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939212.1:n.410+14236T>G
XR_939214.1:n.392+14236T>G
XR_939214.2:n.392+14236T>G