Canonical Allele Identifier: CA557394852
Gene: SLC25A4 HGNC NCBI

Linked Data

dbSNP Id: rs1183020360
gnomAD v2: 4-186065905-T-A
gnomAD v3: 4-185144751-T-A
gnomAD v4: 4-185144751-T-A
MyVariant Identifiers: chr4:g.186065905T>A (hg19) chr4:g.185144751T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144751T>A , CM000666.2:g.185144751T>A GRCh38
NC_000004.11:g.186065905T>A , CM000666.1:g.186065905T>A GRCh37
NC_000004.10:g.186302899T>A NCBI36
NG_013001.1:g.6489T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.112-13T>A MANE Select ENSP00000281456.5:n.112-13T>A
ENST00000281456.10:c.112-13T>A ENSP00000281456.5:n.112-13T>A
ENST00000491736.1:c.112-13T>A ENSP00000476711.1:n.112-13T>A
NM_001151.3:c.112-13T>A NP_001142.2:n.112-13T>A
NM_001151.4:c.112-13T>A MANE Select NP_001142.2:n.112-13T>A
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