Canonical Allele Identifier: CA1105629445
Gene: SLC26A4 HGNC NCBI

Linked Data

dbSNP Id: rs1562847134
gnomAD v3: 7-107717318-G-A
gnomAD v4: 7-107717318-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107717318G>A , CM000669.2:g.107717318G>A GRCh38
NC_000007.13:g.107357763G>A , CM000669.1:g.107357763G>A GRCh37
NC_000007.12:g.107144999G>A NCBI36
NG_008489.1:g.61684G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000644269.2:c.*1872G>A MANE Select ENSP00000494017.1:n.*1872G>A
ENST00000644846.1:c.2871G>A
ENST00000265715.7:c.*1872G>A ENSP00000265715.3:n.*1872G>A
NM_000441.1:c.*1872G>A NP_000432.1:n.*1872G>A
NM_000441.2:c.*1872G>A MANE Select NP_000432.1:n.*1872G>A
Search 100 bp 5'
Search 100 bp 3'