Canonical Allele Identifier: CA1519346839
Gene: SLC25A4 HGNC NCBI

Linked Data

dbSNP Id: rs1579209281
gnomAD v4: 4-185144673-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185144673A>T , CM000666.2:g.185144673A>T GRCh38
NC_000004.11:g.186065827A>T , CM000666.1:g.186065827A>T GRCh37
NC_000004.10:g.186302821A>T NCBI36
NG_013001.1:g.6411A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.112-91A>T MANE Select ENSP00000281456.5:n.112-91A>T
ENST00000281456.10:c.112-91A>T ENSP00000281456.5:n.112-91A>T
ENST00000491736.1:c.112-91A>T ENSP00000476711.1:n.112-91A>T
NM_001151.3:c.112-91A>T NP_001142.2:n.112-91A>T
NM_001151.4:c.112-91A>T MANE Select NP_001142.2:n.112-91A>T
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