Canonical Allele Identifier: CA1496030178
Gene:

Linked Data

dbSNP Id: rs1728166205

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.134601580G>A , CM000666.2:g.134601580G>A GRCh38
NC_000004.11:g.135522735G>A , CM000666.1:g.135522735G>A GRCh37
NC_000004.10:g.135742185G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939212.1:n.410+14221G>A
XR_939214.1:n.392+14221G>A
XR_939214.2:n.392+14221G>A