Canonical Allele Identifier: CA442615168
Gene: SLC25A4 HGNC NCBI

Linked Data

dbSNP Id: rs1168733933
MyVariant Identifiers: chr4:g.186065947T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144793T>A , CM000666.2:g.185144793T>A GRCh38
NC_000004.11:g.186065947T>A , CM000666.1:g.186065947T>A GRCh37
NC_000004.10:g.186302941T>A NCBI36
NG_013001.1:g.6531T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.141T>A MANE Select ENSP00000281456.5:p.Ala47=
ENST00000281456.10:c.141T>A ENSP00000281456.5:p.Ala47=
ENST00000491736.1:c.141T>A ENSP00000476711.1:p.Ala47=
NM_001151.3:c.141T>A NP_001142.2:p.Ala47=
NM_001151.4:c.141T>A MANE Select NP_001142.2:p.Ala47=
Search 100 bp 5'
Search 100 bp 3'