Canonical Allele Identifier: CA358895696
Gene: SLC25A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.186064548T>G (hg19) chr4:g.185143394T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185143394T>G , CM000666.2:g.185143394T>G GRCh38
NC_000004.11:g.186064548T>G , CM000666.1:g.186064548T>G GRCh37
NC_000004.10:g.186301542T>G NCBI36
NG_013001.1:g.5132T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.22T>G MANE Select ENSP00000281456.5:p.Phe8Val
ENST00000281456.10:c.22T>G ENSP00000281456.5:p.Phe8Val
ENST00000491736.1:c.22T>G ENSP00000476711.1:p.Phe8Val
NM_001151.3:c.22T>G NP_001142.2:p.Phe8Val
NM_001151.4:c.22T>G MANE Select NP_001142.2:p.Phe8Val
Search 100 bp 5'
Search 100 bp 3'