Canonical Allele Identifier: CA831178959
Gene: SLC26A4 HGNC NCBI

Linked Data

dbSNP Id: rs1430044525
MyVariant Identifiers: chr7:g.107357773T>G (hg19) chr7:g.107717328T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107717328T>G , CM000669.2:g.107717328T>G GRCh38
NC_000007.13:g.107357773T>G , CM000669.1:g.107357773T>G GRCh37
NC_000007.12:g.107145009T>G NCBI36
NG_008489.1:g.61694T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.*1882T>G MANE Select ENSP00000494017.1:n.*1882T>G
ENST00000644846.1:c.2881T>G
ENST00000265715.7:c.*1882T>G ENSP00000265715.3:n.*1882T>G
NM_000441.1:c.*1882T>G NP_000432.1:n.*1882T>G
NM_000441.2:c.*1882T>G MANE Select NP_000432.1:n.*1882T>G
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