Canonical Allele Identifier: CA1519346831
Gene: SLC25A4 HGNC NCBI

Linked Data

dbSNP Id: rs1734405209
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144667A>G , CM000666.2:g.185144667A>G GRCh38
NC_000004.11:g.186065821A>G , CM000666.1:g.186065821A>G GRCh37
NC_000004.10:g.186302815A>G NCBI36
NG_013001.1:g.6405A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.112-97A>G MANE Select ENSP00000281456.5:n.112-97A>G
ENST00000281456.10:c.112-97A>G ENSP00000281456.5:n.112-97A>G
ENST00000491736.1:c.112-97A>G ENSP00000476711.1:n.112-97A>G
NM_001151.3:c.112-97A>G NP_001142.2:n.112-97A>G
NM_001151.4:c.112-97A>G MANE Select NP_001142.2:n.112-97A>G
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