Canonical Allele Identifier: CA1732755258
Gene: SLC26A4 HGNC NCBI

Linked Data

dbSNP Id: rs1792318548
gnomAD v4: 7-107715327-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107715327C>A , CM000669.2:g.107715327C>A GRCh38
NC_000007.13:g.107355772C>A , CM000669.1:g.107355772C>A GRCh37
NC_000007.12:g.107143008C>A NCBI36
NG_008489.1:g.59693C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.2320-96C>A MANE Select ENSP00000494017.1:n.2320-96C>A
ENST00000644846.1:c.976-96C>A
ENST00000265715.7:c.2320-96C>A ENSP00000265715.3:n.2320-96C>A
ENST00000492030.2:n.506-96C>A
NM_000441.1:c.2320-96C>A NP_000432.1:n.2320-96C>A
XM_005250425.1:c.2320-96C>A XP_005250482.1:n.2320-96C>A
XM_005250425.2:c.2320-96C>A XP_005250482.1:n.2320-96C>A
XM_017012318.1:c.2242-96C>A XP_016867807.1:n.2242-96C>A
NM_000441.2:c.2320-96C>A MANE Select NP_000432.1:n.2320-96C>A
Search 100 bp 5'
Search 100 bp 3'