Canonical Allele Identifier: CA358896047
Gene: SLC25A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.186065982T>G (hg19) chr4:g.185144828T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144828T>G , CM000666.2:g.185144828T>G GRCh38
NC_000004.11:g.186065982T>G , CM000666.1:g.186065982T>G GRCh37
NC_000004.10:g.186302976T>G NCBI36
NG_013001.1:g.6566T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.176T>G MANE Select ENSP00000281456.5:p.Val59Gly
ENST00000281456.10:c.176T>G ENSP00000281456.5:p.Val59Gly
ENST00000491736.1:c.176T>G ENSP00000476711.1:p.Val59Gly
NM_001151.3:c.176T>G NP_001142.2:p.Val59Gly
NM_001151.4:c.176T>G MANE Select NP_001142.2:p.Val59Gly
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Search 100 bp 3'