Canonical Allele Identifier: CA358895697
Gene: SLC25A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.186064549T>A (hg19) chr4:g.185143395T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185143395T>A , CM000666.2:g.185143395T>A GRCh38
NC_000004.11:g.186064549T>A , CM000666.1:g.186064549T>A GRCh37
NC_000004.10:g.186301543T>A NCBI36
NG_013001.1:g.5133T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.23T>A MANE Select ENSP00000281456.5:p.Phe8Tyr
ENST00000281456.10:c.23T>A ENSP00000281456.5:p.Phe8Tyr
ENST00000491736.1:c.23T>A ENSP00000476711.1:p.Phe8Tyr
NM_001151.3:c.23T>A NP_001142.2:p.Phe8Tyr
NM_001151.4:c.23T>A MANE Select NP_001142.2:p.Phe8Tyr
Search 100 bp 5'
Search 100 bp 3'