Canonical Allele Identifier: CA831178121
Gene: SLC26A4 HGNC NCBI

Linked Data

dbSNP Id: rs1445751500
gnomAD v3: 7-107716007-A-T
gnomAD v4: 7-107716007-A-T
MyVariant Identifiers: chr7:g.107356452A>T (hg19) chr7:g.107716007A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107716007A>T , CM000669.2:g.107716007A>T GRCh38
NC_000007.13:g.107356452A>T , CM000669.1:g.107356452A>T GRCh37
NC_000007.12:g.107143688A>T NCBI36
NG_008489.1:g.60373A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.*561A>T MANE Select ENSP00000494017.1:n.*561A>T
ENST00000644846.1:c.1560A>T
ENST00000265715.7:c.*561A>T ENSP00000265715.3:n.*561A>T
NM_000441.1:c.*561A>T NP_000432.1:n.*561A>T
XM_005250425.2:c.*561A>T XP_005250482.1:n.*561A>T
XM_017012318.1:c.*561A>T XP_016867807.1:n.*561A>T
NM_000441.2:c.*561A>T MANE Select NP_000432.1:n.*561A>T
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