Canonical Allele Identifier: CA792209251
Gene: SLC25A4 HGNC NCBI

Linked Data

dbSNP Id: rs1187875908
gnomAD v3: 4-185144649-A-G
gnomAD v4: 4-185144649-A-G
MyVariant Identifiers: chr4:g.186065803A>G (hg19) chr4:g.185144649A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144649A>G , CM000666.2:g.185144649A>G GRCh38
NC_000004.11:g.186065803A>G , CM000666.1:g.186065803A>G GRCh37
NC_000004.10:g.186302797A>G NCBI36
NG_013001.1:g.6387A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.112-115A>G MANE Select ENSP00000281456.5:n.112-115A>G
ENST00000281456.10:c.112-115A>G ENSP00000281456.5:n.112-115A>G
ENST00000491736.1:c.112-115A>G ENSP00000476711.1:n.112-115A>G
NM_001151.3:c.112-115A>G NP_001142.2:n.112-115A>G
NM_001151.4:c.112-115A>G MANE Select NP_001142.2:n.112-115A>G
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