Canonical Allele Identifier: CA2672840608
Gene: SLC25A4 HGNC NCBI

Linked Data

gnomAD v4: 4-185143361-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.185143361C>G , CM000666.2:g.185143361C>G GRCh38
NC_000004.11:g.186064515C>G , CM000666.1:g.186064515C>G GRCh37
NC_000004.10:g.186301509C>G NCBI36
NG_013001.1:g.5099C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000281456.11:c.-12C>G MANE Select ENSP00000281456.5:n.-12C>G
ENST00000281456.10:c.-12C>G ENSP00000281456.5:n.-12C>G
ENST00000491736.1:c.-12C>G ENSP00000476711.1:n.-12C>G
NM_001151.3:c.-12C>G NP_001142.2:n.-12C>G
NM_001151.4:c.-12C>G MANE Select NP_001142.2:n.-12C>G
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