Canonical Allele Identifier: CA358896337
Gene: SLC25A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.186066107G>C (hg19) chr4:g.185144953G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144953G>C , CM000666.2:g.185144953G>C GRCh38
NC_000004.11:g.186066107G>C , CM000666.1:g.186066107G>C GRCh37
NC_000004.10:g.186303101G>C NCBI36
NG_013001.1:g.6691G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.301G>C MANE Select ENSP00000281456.5:p.Gly101Arg
ENST00000281456.10:c.301G>C ENSP00000281456.5:p.Gly101Arg
ENST00000491736.1:c.301G>C ENSP00000476711.1:p.Gly101Arg
NM_001151.3:c.301G>C NP_001142.2:p.Gly101Arg
NM_001151.4:c.301G>C MANE Select NP_001142.2:p.Gly101Arg
Search 100 bp 5'
Search 100 bp 3'