Canonical Allele Identifier: CA3156428
Gene: SLC25A4 HGNC NCBI

Linked Data

dbSNP Id: rs761178878
ExAC: 4:186065914 C / G
gnomAD v2: 4-186065914-C-G
gnomAD v4: 4-185144760-C-G
MyVariant Identifiers: chr4:g.186065914C>G (hg19) chr4:g.185144760C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144760C>G , CM000666.2:g.185144760C>G GRCh38
NC_000004.11:g.186065914C>G , CM000666.1:g.186065914C>G GRCh37
NC_000004.10:g.186302908C>G NCBI36
NG_013001.1:g.6498C>G

Transcript Alleles

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