Canonical Allele Identifier: CA22539492
Gene: SLC25A3P1 HGNC NCBI

Linked Data

dbSNP Id: rs370142404
MyVariant Identifiers: chr1:g.53884483C>T (hg19) chr1:g.53418811C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.53418811C>T , CM000663.2:g.53418811C>T GRCh38
NC_000001.10:g.53884483C>T , CM000663.1:g.53884483C>T GRCh37
NC_000001.9:g.53657071C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000563752.5:n.202-1145G>A
XR_426691.2:n.27-1145G>A
XR_426692.2:n.20-1145G>A
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