Canonical Allele Identifier: CA132649
Gene: SLC26A4 HGNC NCBI
SLC26A4-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 43487
dbSNP Id: rs17154282

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107660793C>G , CM000669.2:g.107660793C>G GRCh38
NC_000007.13:g.107301238C>G , CM000669.1:g.107301238C>G GRCh37
NC_000007.12:g.107088474C>G NCBI36
NG_008489.1:g.5159C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000265715.7:c.-66C>G (SLC26A4) ENSP00000265715.3:n.-66C>G
NM_000441.1:c.-66C>G (SLC26A4) NP_000432.1:n.-66C>G
NR_028137.1:n.198-587G>C (SLC26A4-AS1)