Canonical Allele Identifier: CA1105629509
Gene: SLC26A4 HGNC NCBI

Linked Data

gnomAD v3: 7-107717330-C-T
gnomAD v4: 7-107717330-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107717330C>T , CM000669.2:g.107717330C>T GRCh38
NC_000007.13:g.107357775C>T , CM000669.1:g.107357775C>T GRCh37
NC_000007.12:g.107145011C>T NCBI36
NG_008489.1:g.61696C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.*1884C>T MANE Select ENSP00000494017.1:n.*1884C>T
ENST00000644846.1:c.2883C>T
ENST00000265715.7:c.*1884C>T ENSP00000265715.3:n.*1884C>T
NM_000441.1:c.*1884C>T NP_000432.1:n.*1884C>T
NM_000441.2:c.*1884C>T MANE Select NP_000432.1:n.*1884C>T
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