Canonical Allele Identifier: CA368845896
Gene: SLC26A4 HGNC NCBI

Linked Data

dbSNP Id: rs1562843570
gnomAD v2: 7-107350582-G-A
gnomAD v4: 7-107710137-G-A
MyVariant Identifiers: chr7:g.107350582G>A (hg19) chr7:g.107710137G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107710137G>A , CM000669.2:g.107710137G>A GRCh38
NC_000007.13:g.107350582G>A , CM000669.1:g.107350582G>A GRCh37
NC_000007.12:g.107137818G>A NCBI36
NG_008489.1:g.54503G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.2173G>A MANE Select ENSP00000494017.1:p.Ala725Thr
ENST00000644846.1:c.829G>A
ENST00000265715.7:c.2173G>A ENSP00000265715.3:p.Ala725Thr
ENST00000492030.2:n.377-18G>A
NM_000441.1:c.2173G>A NP_000432.1:p.Ala725Thr
XM_005250425.1:c.2173G>A XP_005250482.1:p.Ala725Thr
XM_005250425.2:c.2173G>A XP_005250482.1:p.Ala725Thr
XM_017012318.1:c.2095G>A XP_016867807.1:p.Ala699Thr
NM_000441.2:c.2173G>A MANE Select NP_000432.1:p.Ala725Thr
Search 100 bp 5'
Search 100 bp 3'