Canonical Allele Identifier: CA164232497
Gene: SLC26A4 HGNC NCBI

Linked Data

dbSNP Id: rs892989505
gnomAD v3: 7-107716070-C-G
gnomAD v4: 7-107716070-C-G
MyVariant Identifiers: chr7:g.107356515C>G (hg19) chr7:g.107716070C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107716070C>G , CM000669.2:g.107716070C>G GRCh38
NC_000007.13:g.107356515C>G , CM000669.1:g.107356515C>G GRCh37
NC_000007.12:g.107143751C>G NCBI36
NG_008489.1:g.60436C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.*624C>G MANE Select ENSP00000494017.1:n.*624C>G
ENST00000644846.1:c.1623C>G
ENST00000265715.7:c.*624C>G ENSP00000265715.3:n.*624C>G
NM_000441.1:c.*624C>G NP_000432.1:n.*624C>G
XM_005250425.2:c.*624C>G XP_005250482.1:n.*624C>G
XM_017012318.1:c.*624C>G XP_016867807.1:n.*624C>G
NM_000441.2:c.*624C>G MANE Select NP_000432.1:n.*624C>G
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