Canonical Allele Identifier: CA1167297765
Gene: SLC25A3P1 HGNC NCBI

Linked Data

dbSNP Id: rs1776421

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53418785C>A , CM000663.2:g.53418785C>A GRCh38
NC_000001.10:g.53884457C>A , CM000663.1:g.53884457C>A GRCh37
NC_000001.9:g.53657045C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000563752.5:n.202-1119G>T
XR_426691.2:n.27-1119G>T
XR_426692.2:n.20-1119G>T