Canonical Allele Identifier: CA1001819534
Gene: SLC25A3P1 HGNC NCBI

Linked Data

dbSNP Id: rs1656910437
gnomAD v3: 1-53418830-T-C
gnomAD v4: 1-53418830-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53418830T>C , CM000663.2:g.53418830T>C GRCh38
NC_000001.10:g.53884502T>C , CM000663.1:g.53884502T>C GRCh37
NC_000001.9:g.53657090T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000563752.5:n.202-1164A>G
XR_426691.2:n.27-1164A>G
XR_426692.2:n.20-1164A>G
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