Canonical Allele Identifier: CA2684469899
Gene: SLC26A4 HGNC NCBI

Linked Data

gnomAD v4: 7-107717456-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107717456G>T , CM000669.2:g.107717456G>T GRCh38
NC_000007.13:g.107357901G>T , CM000669.1:g.107357901G>T GRCh37
NC_000007.12:g.107145137G>T NCBI36
NG_008489.1:g.61822G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.*2010G>T MANE Select ENSP00000494017.1:n.*2010G>T
ENST00000265715.7:c.*2010G>T ENSP00000265715.3:n.*2010G>T
NM_000441.1:c.*2010G>T NP_000432.1:n.*2010G>T
NM_000441.2:c.*2010G>T MANE Select NP_000432.1:n.*2010G>T
Search 100 bp 5'
Search 100 bp 3'