Canonical Allele Identifier: CA10770535

Gene: SLC25A3P1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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