Canonical Allele Identifier: CA358896033
Gene: SLC25A4 HGNC NCBI

Linked Data

dbSNP Id: rs1734408523
gnomAD v4: 4-185144822-G-A
MyVariant Identifiers: chr4:g.186065976G>A (hg19) chr4:g.185144822G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144822G>A , CM000666.2:g.185144822G>A GRCh38
NC_000004.11:g.186065976G>A , CM000666.1:g.186065976G>A GRCh37
NC_000004.10:g.186302970G>A NCBI36
NG_013001.1:g.6560G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.170G>A MANE Select ENSP00000281456.5:p.Cys57Tyr
ENST00000281456.10:c.170G>A ENSP00000281456.5:p.Cys57Tyr
ENST00000491736.1:c.170G>A ENSP00000476711.1:p.Cys57Tyr
NM_001151.3:c.170G>A NP_001142.2:p.Cys57Tyr
NM_001151.4:c.170G>A MANE Select NP_001142.2:p.Cys57Tyr
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