Canonical Allele Identifier: CA127986
Gene: SLC25A4 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 18247
ClinVar RCV Id: RCV000019909
dbSNP Id: rs104893876

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144945T>C , CM000666.2:g.185144945T>C GRCh38
NC_000004.10:g.186303093T>C NCBI36
NC_000004.11:g.186066099T>C , CM000666.1:g.186066099T>C GRCh37
NG_013001.1:g.6683T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000281456.10:c.293T>C ENSP00000281456.5:p.Leu98Pro
ENST00000491736.1:c.293T>C ENSP00000476711.1:p.Leu98Pro
NM_001151.3:c.293T>C NP_001142.2:p.Leu98Pro