Canonical Allele Identifier: CA1732742017
Gene: SLC26A4 HGNC NCBI

Linked Data

dbSNP Id: rs1791313775
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107683538dup , CM000669.2:g.107683538dup GRCh38
NC_000007.13:g.107323983dup , CM000669.1:g.107323983dup GRCh37
NC_000007.12:g.107111219dup NCBI36
NG_008489.1:g.27904dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1001+1dup
ENST00000265715.7:c.1001+1dup
NM_000441.1:c.1001+1dup
XM_005250425.1:c.1001+1dup
XM_006716025.2:c.1001+1dup
XM_005250425.2:c.1001+1dup
XM_006716025.3:c.1001+1dup
XM_017012318.1:c.1001+1dup
NM_000441.2:c.1001+1dup
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