Canonical Allele Identifier: CA442615217
Gene: SLC25A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.186066040G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144886G>A , CM000666.2:g.185144886G>A GRCh38
NC_000004.11:g.186066040G>A , CM000666.1:g.186066040G>A GRCh37
NC_000004.10:g.186303034G>A NCBI36
NG_013001.1:g.6624G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.234G>A MANE Select ENSP00000281456.5:p.Val78=
ENST00000281456.10:c.234G>A ENSP00000281456.5:p.Val78=
ENST00000491736.1:c.234G>A ENSP00000476711.1:p.Val78=
NM_001151.3:c.234G>A NP_001142.2:p.Val78=
NM_001151.4:c.234G>A MANE Select NP_001142.2:p.Val78=
Search 100 bp 5'
Search 100 bp 3'