Canonical Allele Identifier: CA112004181
Gene: SLC25A4 HGNC NCBI

Linked Data

dbSNP Id: rs183128370
gnomAD v2: 4-186064443-C-T
gnomAD v3: 4-185143289-C-T
gnomAD v4: 4-185143289-C-T
MyVariant Identifiers: chr4:g.186064443C>T (hg19) chr4:g.185143289C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185143289C>T , CM000666.2:g.185143289C>T GRCh38
NC_000004.11:g.186064443C>T , CM000666.1:g.186064443C>T GRCh37
NC_000004.10:g.186301437C>T NCBI36
NG_013001.1:g.5027C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.-84C>T MANE Select ENSP00000281456.5:n.-84C>T
ENST00000281456.10:c.-84C>T ENSP00000281456.5:n.-84C>T
ENST00000491736.1:c.-84C>T ENSP00000476711.1:n.-84C>T
NM_001151.3:c.-84C>T NP_001142.2:n.-84C>T
NM_001151.4:c.-84C>T MANE Select NP_001142.2:n.-84C>T
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