Canonical Allele Identifier: CA557394794
Gene: SLC25A4 HGNC NCBI

Linked Data

dbSNP Id: rs1379120493
gnomAD v2: 4-186065842-A-C
gnomAD v3: 4-185144688-A-C
gnomAD v4: 4-185144688-A-C
MyVariant Identifiers: chr4:g.186065842A>C (hg19) chr4:g.185144688A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144688A>C , CM000666.2:g.185144688A>C GRCh38
NC_000004.11:g.186065842A>C , CM000666.1:g.186065842A>C GRCh37
NC_000004.10:g.186302836A>C NCBI36
NG_013001.1:g.6426A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.112-76A>C MANE Select ENSP00000281456.5:n.112-76A>C
ENST00000281456.10:c.112-76A>C ENSP00000281456.5:n.112-76A>C
ENST00000491736.1:c.112-76A>C ENSP00000476711.1:n.112-76A>C
NM_001151.3:c.112-76A>C NP_001142.2:n.112-76A>C
NM_001151.4:c.112-76A>C MANE Select NP_001142.2:n.112-76A>C
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