Canonical Allele Identifier: CA577030994
Gene: SLC26A4 HGNC NCBI

Linked Data

dbSNP Id: rs1411908322
gnomAD v2: 7-107357769-C-T
gnomAD v3: 7-107717324-C-T
gnomAD v4: 7-107717324-C-T
MyVariant Identifiers: chr7:g.107357769C>T (hg19) chr7:g.107717324C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107717324C>T , CM000669.2:g.107717324C>T GRCh38
NC_000007.13:g.107357769C>T , CM000669.1:g.107357769C>T GRCh37
NC_000007.12:g.107145005C>T NCBI36
NG_008489.1:g.61690C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.*1878C>T MANE Select ENSP00000494017.1:n.*1878C>T
ENST00000644846.1:c.2877C>T
ENST00000265715.7:c.*1878C>T ENSP00000265715.3:n.*1878C>T
NM_000441.1:c.*1878C>T NP_000432.1:n.*1878C>T
NM_000441.2:c.*1878C>T MANE Select NP_000432.1:n.*1878C>T
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