Canonical Allele Identifier: CA358896050
Gene: SLC25A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.186065985G>T (hg19) chr4:g.185144831G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144831G>T , CM000666.2:g.185144831G>T GRCh38
NC_000004.11:g.186065985G>T , CM000666.1:g.186065985G>T GRCh37
NC_000004.10:g.186302979G>T NCBI36
NG_013001.1:g.6569G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.179G>T MANE Select ENSP00000281456.5:p.Arg60Ile
ENST00000281456.10:c.179G>T ENSP00000281456.5:p.Arg60Ile
ENST00000491736.1:c.179G>T ENSP00000476711.1:p.Arg60Ile
NM_001151.3:c.179G>T NP_001142.2:p.Arg60Ile
NM_001151.4:c.179G>T MANE Select NP_001142.2:p.Arg60Ile
Search 100 bp 5'
Search 100 bp 3'