Canonical Allele Identifier: CA4433026
Gene: SLC26A4 HGNC NCBI

Linked Data

dbSNP Id: rs753682653
ExAC: 7:107344833 A / C
gnomAD v2: 7-107344833-A-C
gnomAD v3: 7-107704388-A-C
gnomAD v4: 7-107704388-A-C
MyVariant Identifiers: chr7:g.107344833A>C (hg19) chr7:g.107704388A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107704388A>C , CM000669.2:g.107704388A>C GRCh38
NC_000007.13:g.107344833A>C , CM000669.1:g.107344833A>C GRCh37
NC_000007.12:g.107132069A>C NCBI36
NG_008489.1:g.48754A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.2089+3A>C MANE Select ENSP00000494017.1:n.2089+3A>C
ENST00000644846.1:c.745+2331A>C
ENST00000265715.7:c.2089+3A>C ENSP00000265715.3:n.2089+3A>C
ENST00000492030.2:n.376+3A>C
NM_000441.1:c.2089+3A>C NP_000432.1:n.2089+3A>C
XM_005250425.1:c.2089+3A>C XP_005250482.1:n.2089+3A>C
XM_005250425.2:c.2089+3A>C XP_005250482.1:n.2089+3A>C
XM_017012318.1:c.2011+3A>C XP_016867807.1:n.2011+3A>C
NM_000441.2:c.2089+3A>C MANE Select NP_000432.1:n.2089+3A>C
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