Canonical Allele Identifier: CA457104191
Gene: SLC26A4 HGNC NCBI

Linked Data

gnomAD v4: 7-107704393-C-A
MyVariant Identifiers: chr7:g.107344838C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107704393C>A , CM000669.2:g.107704393C>A GRCh38
NC_000007.13:g.107344838C>A , CM000669.1:g.107344838C>A GRCh37
NC_000007.12:g.107132074C>A NCBI36
NG_008489.1:g.48759C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.2089+8C>A MANE Select ENSP00000494017.1:n.2089+8C>A
ENST00000644846.1:c.745+2336C>A
ENST00000265715.7:c.2089+8C>A ENSP00000265715.3:n.2089+8C>A
ENST00000492030.2:n.376+8C>A
NM_000441.1:c.2089+8C>A NP_000432.1:n.2089+8C>A
XM_005250425.1:c.2089+8C>A XP_005250482.1:n.2089+8C>A
XM_005250425.2:c.2089+8C>A XP_005250482.1:n.2089+8C>A
XM_017012318.1:c.2011+8C>A XP_016867807.1:n.2011+8C>A
NM_000441.2:c.2089+8C>A MANE Select NP_000432.1:n.2089+8C>A
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