Canonical Allele Identifier: CA1001819524
Gene: SLC25A3P1 HGNC NCBI

Linked Data

dbSNP Id: rs1656910152
gnomAD v3: 1-53418794-A-G
gnomAD v4: 1-53418794-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53418794A>G , CM000663.2:g.53418794A>G GRCh38
NC_000001.10:g.53884466A>G , CM000663.1:g.53884466A>G GRCh37
NC_000001.9:g.53657054A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000563752.5:n.202-1128T>C
XR_426691.2:n.27-1128T>C
XR_426692.2:n.20-1128T>C