Canonical Allele Identifier: CA1105629930
Gene: SLC26A4 HGNC NCBI

Linked Data

dbSNP Id: rs1584351276
gnomAD v3: 7-107717422-T-A
gnomAD v4: 7-107717422-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107717422T>A , CM000669.2:g.107717422T>A GRCh38
NC_000007.13:g.107357867T>A , CM000669.1:g.107357867T>A GRCh37
NC_000007.12:g.107145103T>A NCBI36
NG_008489.1:g.61788T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.*1976T>A MANE Select ENSP00000494017.1:n.*1976T>A
ENST00000265715.7:c.*1976T>A ENSP00000265715.3:n.*1976T>A
NM_000441.1:c.*1976T>A NP_000432.1:n.*1976T>A
NM_000441.2:c.*1976T>A MANE Select NP_000432.1:n.*1976T>A
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