Canonical Allele Identifier: CA577030993
Gene: SLC26A4 HGNC NCBI

Linked Data

dbSNP Id: rs1160621150
gnomAD v2: 7-107357752-A-G
gnomAD v3: 7-107717307-A-G
gnomAD v4: 7-107717307-A-G
MyVariant Identifiers: chr7:g.107357752A>G (hg19) chr7:g.107717307A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107717307A>G , CM000669.2:g.107717307A>G GRCh38
NC_000007.13:g.107357752A>G , CM000669.1:g.107357752A>G GRCh37
NC_000007.12:g.107144988A>G NCBI36
NG_008489.1:g.61673A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.*1861A>G MANE Select ENSP00000494017.1:n.*1861A>G
ENST00000644846.1:c.2860A>G
ENST00000265715.7:c.*1861A>G ENSP00000265715.3:n.*1861A>G
NM_000441.1:c.*1861A>G NP_000432.1:n.*1861A>G
NM_000441.2:c.*1861A>G MANE Select NP_000432.1:n.*1861A>G
Search 100 bp 5'
Search 100 bp 3'