Canonical Allele Identifier: CA106421596
Gene:

Linked Data

dbSNP Id: rs937296920

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134601486G>A , CM000666.2:g.134601486G>A GRCh38
NC_000004.11:g.135522641G>A , CM000666.1:g.135522641G>A GRCh37
NC_000004.10:g.135742091G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939212.1:n.410+14127G>A
XR_939214.1:n.392+14127G>A
XR_939214.2:n.392+14127G>A