Canonical Allele Identifier: CA1732756966
Gene: SLC26A4 HGNC NCBI

Linked Data

dbSNP Id: rs1584351090
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107717319T>G , CM000669.2:g.107717319T>G GRCh38
NC_000007.13:g.107357764T>G , CM000669.1:g.107357764T>G GRCh37
NC_000007.12:g.107145000T>G NCBI36
NG_008489.1:g.61685T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.*1873T>G MANE Select ENSP00000494017.1:n.*1873T>G
ENST00000644846.1:c.2872T>G
ENST00000265715.7:c.*1873T>G ENSP00000265715.3:n.*1873T>G
NM_000441.1:c.*1873T>G NP_000432.1:n.*1873T>G
NM_000441.2:c.*1873T>G MANE Select NP_000432.1:n.*1873T>G
Search 100 bp 5'
Search 100 bp 3'