Canonical Allele Identifier: CA2684468686
Gene: SLC26A4 HGNC NCBI

Linked Data

gnomAD v4: 7-107701039-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107701039A>C , CM000669.2:g.107701039A>C GRCh38
NC_000007.13:g.107341484A>C , CM000669.1:g.107341484A>C GRCh37
NC_000007.12:g.107128720A>C NCBI36
NG_008489.1:g.45405A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.1708-62A>C MANE Select ENSP00000494017.1:n.1708-62A>C
ENST00000644846.1:c.419-62A>C
ENST00000265715.7:c.1708-62A>C ENSP00000265715.3:n.1708-62A>C
ENST00000480841.5:n.557-62A>C
ENST00000492030.2:n.91-788A>C
NM_000441.1:c.1708-62A>C NP_000432.1:n.1708-62A>C
XM_005250425.1:c.1708-62A>C XP_005250482.1:n.1708-62A>C
XM_005250425.2:c.1708-62A>C XP_005250482.1:n.1708-62A>C
XM_017012318.1:c.1630-62A>C XP_016867807.1:n.1630-62A>C
NM_000441.2:c.1708-62A>C MANE Select NP_000432.1:n.1708-62A>C
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