Canonical Allele Identifier: CA1167297788
Gene: SLC25A3P1 HGNC NCBI

Linked Data

dbSNP Id: rs1656910490

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53418833T>C , CM000663.2:g.53418833T>C GRCh38
NC_000001.10:g.53884505T>C , CM000663.1:g.53884505T>C GRCh37
NC_000001.9:g.53657093T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000563752.5:n.202-1167A>G
XR_426691.2:n.27-1167A>G
XR_426692.2:n.20-1167A>G