Canonical Allele Identifier: CA2672840939
Gene: SLC25A4 HGNC NCBI

Linked Data

dbSNP Id: rs1282065046
gnomAD v4: 4-185144731-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144731C>A , CM000666.2:g.185144731C>A GRCh38
NC_000004.11:g.186065885C>A , CM000666.1:g.186065885C>A GRCh37
NC_000004.10:g.186302879C>A NCBI36
NG_013001.1:g.6469C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.112-33C>A MANE Select ENSP00000281456.5:n.112-33C>A
ENST00000281456.10:c.112-33C>A ENSP00000281456.5:n.112-33C>A
ENST00000491736.1:c.112-33C>A ENSP00000476711.1:n.112-33C>A
NM_001151.3:c.112-33C>A NP_001142.2:n.112-33C>A
NM_001151.4:c.112-33C>A MANE Select NP_001142.2:n.112-33C>A
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