Canonical Allele Identifier: CA106421611
Gene:

Linked Data

dbSNP Id: rs376035381

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134601518G>A , CM000666.2:g.134601518G>A GRCh38
NC_000004.11:g.135522673G>A , CM000666.1:g.135522673G>A GRCh37
NC_000004.10:g.135742123G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939212.1:n.410+14159G>A
XR_939214.1:n.392+14159G>A
XR_939214.2:n.392+14159G>A