Canonical Allele Identifier: CA1105629471
Gene: SLC26A4 HGNC NCBI

Linked Data

gnomAD v3: 7-107717321-G-A
gnomAD v4: 7-107717321-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107717321G>A , CM000669.2:g.107717321G>A GRCh38
NC_000007.13:g.107357766G>A , CM000669.1:g.107357766G>A GRCh37
NC_000007.12:g.107145002G>A NCBI36
NG_008489.1:g.61687G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.*1875G>A MANE Select ENSP00000494017.1:n.*1875G>A
ENST00000644846.1:c.2874G>A
ENST00000265715.7:c.*1875G>A ENSP00000265715.3:n.*1875G>A
NM_000441.1:c.*1875G>A NP_000432.1:n.*1875G>A
NM_000441.2:c.*1875G>A MANE Select NP_000432.1:n.*1875G>A
Search 100 bp 5'
Search 100 bp 3'