Canonical Allele Identifier: CA457102066
Gene: SLC26A4 HGNC NCBI

Linked Data

dbSNP Id: rs1370506027
gnomAD v2: 7-107341579-A-C
gnomAD v3: 7-107701134-A-C
gnomAD v4: 7-107701134-A-C
MyVariant Identifiers: chr7:g.107341579A>C (hg19) chr7:g.107701134A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107701134A>C , CM000669.2:g.107701134A>C GRCh38
NC_000007.13:g.107341579A>C , CM000669.1:g.107341579A>C GRCh37
NC_000007.12:g.107128815A>C NCBI36
NG_008489.1:g.45500A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.1741A>C MANE Select ENSP00000494017.1:p.Arg581=
ENST00000644846.1:c.452A>C
ENST00000265715.7:c.1741A>C ENSP00000265715.3:p.Arg581=
ENST00000480841.5:n.590A>C
ENST00000492030.2:n.91-693A>C
NM_000441.1:c.1741A>C NP_000432.1:p.Arg581=
XM_005250425.1:c.1741A>C XP_005250482.1:p.Arg581=
XM_005250425.2:c.1741A>C XP_005250482.1:p.Arg581=
XM_017012318.1:c.1663A>C XP_016867807.1:p.Arg555=
NM_000441.2:c.1741A>C MANE Select NP_000432.1:p.Arg581=
Search 100 bp 5'
Search 100 bp 3'