Canonical Allele Identifier: CA358896338
Gene: SLC25A4 HGNC NCBI

Linked Data

dbSNP Id: rs1271723621
gnomAD v2: 4-186066107-G-A
gnomAD v4: 4-185144953-G-A
MyVariant Identifiers: chr4:g.186066107G>A (hg19) chr4:g.185144953G>A (hg38)
JSON-LD

Genomic Alleles

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

Transcript Alleles

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