Canonical Allele Identifier: CA22539491
Gene: SLC25A3P1 HGNC NCBI

Linked Data

dbSNP Id: rs955343626
gnomAD v3: 1-53418810-T-G
gnomAD v4: 1-53418810-T-G
MyVariant Identifiers: chr1:g.53884482T>G (hg19) chr1:g.53418810T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53418810T>G , CM000663.2:g.53418810T>G GRCh38
NC_000001.10:g.53884482T>G , CM000663.1:g.53884482T>G GRCh37
NC_000001.9:g.53657070T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000563752.5:n.202-1144A>C
XR_426691.2:n.27-1144A>C
XR_426692.2:n.20-1144A>C
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