Canonical Allele Identifier: CA2684469886
Gene: SLC26A4 HGNC NCBI

Linked Data

gnomAD v4: 7-107717325-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107717325C>G , CM000669.2:g.107717325C>G GRCh38
NC_000007.13:g.107357770C>G , CM000669.1:g.107357770C>G GRCh37
NC_000007.12:g.107145006C>G NCBI36
NG_008489.1:g.61691C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.*1879C>G MANE Select ENSP00000494017.1:n.*1879C>G
ENST00000644846.1:c.2878C>G
ENST00000265715.7:c.*1879C>G ENSP00000265715.3:n.*1879C>G
NM_000441.1:c.*1879C>G NP_000432.1:n.*1879C>G
NM_000441.2:c.*1879C>G MANE Select NP_000432.1:n.*1879C>G
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