Canonical Allele Identifier: CA1732757182
Gene: SLC26A4 HGNC NCBI

Linked Data

dbSNP Id: rs1792375877
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107717451G>A , CM000669.2:g.107717451G>A GRCh38
NC_000007.13:g.107357896G>A , CM000669.1:g.107357896G>A GRCh37
NC_000007.12:g.107145132G>A NCBI36
NG_008489.1:g.61817G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.*2005G>A MANE Select ENSP00000494017.1:n.*2005G>A
ENST00000265715.7:c.*2005G>A ENSP00000265715.3:n.*2005G>A
NM_000441.1:c.*2005G>A NP_000432.1:n.*2005G>A
NM_000441.2:c.*2005G>A MANE Select NP_000432.1:n.*2005G>A
Search 100 bp 5'
Search 100 bp 3'