Canonical Allele Identifier: CA457103254
Gene: SLC26A4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.107342379A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107701934A>G , CM000669.2:g.107701934A>G GRCh38
NC_000007.13:g.107342379A>G , CM000669.1:g.107342379A>G GRCh37
NC_000007.12:g.107129615A>G NCBI36
NG_008489.1:g.46300A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.1911A>G MANE Select ENSP00000494017.1:p.Gln637=
ENST00000644846.1:c.622A>G
ENST00000265715.7:c.1911A>G ENSP00000265715.3:p.Gln637=
ENST00000492030.2:n.198A>G
NM_000441.1:c.1911A>G NP_000432.1:p.Gln637=
XM_005250425.1:c.1911A>G XP_005250482.1:p.Gln637=
XM_005250425.2:c.1911A>G XP_005250482.1:p.Gln637=
XM_017012318.1:c.1833A>G XP_016867807.1:p.Gln611=
NM_000441.2:c.1911A>G MANE Select NP_000432.1:p.Gln637=
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