Canonical Allele Identifier: CA1732755775
Gene: SLC26A4 HGNC NCBI

Linked Data

dbSNP Id: rs1584349981
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107715989A>G , CM000669.2:g.107715989A>G GRCh38
NC_000007.13:g.107356434A>G , CM000669.1:g.107356434A>G GRCh37
NC_000007.12:g.107143670A>G NCBI36
NG_008489.1:g.60355A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.*543A>G MANE Select ENSP00000494017.1:n.*543A>G
ENST00000644846.1:c.1542A>G
ENST00000265715.7:c.*543A>G ENSP00000265715.3:n.*543A>G
NM_000441.1:c.*543A>G NP_000432.1:n.*543A>G
XM_005250425.2:c.*543A>G XP_005250482.1:n.*543A>G
XM_017012318.1:c.*543A>G XP_016867807.1:n.*543A>G
NM_000441.2:c.*543A>G MANE Select NP_000432.1:n.*543A>G
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