Canonical Allele Identifier: CA831183731
Gene: SLC26A4 HGNC NCBI

Linked Data

dbSNP Id: rs1358531150
MyVariant Identifiers: chr7:g.107336792T>G (hg19) chr7:g.107696347T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107696347T>G , CM000669.2:g.107696347T>G GRCh38
NC_000007.13:g.107336792T>G , CM000669.1:g.107336792T>G GRCh37
NC_000007.12:g.107124028T>G NCBI36
NG_008489.1:g.40713T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.1544+308T>G MANE Select ENSP00000494017.1:n.1544+308T>G
ENST00000644846.1:c.255+308T>G
ENST00000265715.7:c.1544+308T>G ENSP00000265715.3:n.1544+308T>G
ENST00000477350.5:n.391+308T>G
ENST00000480841.5:n.393+308T>G
NM_000441.1:c.1544+308T>G NP_000432.1:n.1544+308T>G
XM_005250425.1:c.1544+308T>G XP_005250482.1:n.1544+308T>G
XM_005250425.2:c.1544+308T>G XP_005250482.1:n.1544+308T>G
XM_017012318.1:c.1466+308T>G XP_016867807.1:n.1466+308T>G
NM_000441.2:c.1544+308T>G MANE Select NP_000432.1:n.1544+308T>G
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