Canonical Allele Identifier: CA2715578535
Gene: SLC26A4 HGNC NCBI

Linked Data

dbSNP Id: rs2129321360
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107717423G>T , CM000669.2:g.107717423G>T GRCh38
NC_000007.13:g.107357868G>T , CM000669.1:g.107357868G>T GRCh37
NC_000007.12:g.107145104G>T NCBI36
NG_008489.1:g.61789G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.*1977G>T MANE Select ENSP00000494017.1:n.*1977G>T
ENST00000265715.7:c.*1977G>T ENSP00000265715.3:n.*1977G>T
NM_000441.1:c.*1977G>T NP_000432.1:n.*1977G>T
NM_000441.2:c.*1977G>T MANE Select NP_000432.1:n.*1977G>T
Search 100 bp 5'
Search 100 bp 3'