Canonical Allele Identifier: CA457104616
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1532254
ClinVar RCV Id: RCV002106916
dbSNP Id: rs2129319935
MyVariant Identifiers: chr7:g.107350593T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107710148T>C , CM000669.2:g.107710148T>C GRCh38
NC_000007.13:g.107350593T>C , CM000669.1:g.107350593T>C GRCh37
NC_000007.12:g.107137829T>C NCBI36
NG_008489.1:g.54514T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000644269.2:c.2184T>C MANE Select ENSP00000494017.1:p.Tyr728=
ENST00000644846.1:c.840T>C
ENST00000265715.7:c.2184T>C ENSP00000265715.3:p.Tyr728=
ENST00000492030.2:n.377-7T>C
NM_000441.1:c.2184T>C NP_000432.1:p.Tyr728=
XM_005250425.1:c.2184T>C XP_005250482.1:p.Tyr728=
XM_005250425.2:c.2184T>C XP_005250482.1:p.Tyr728=
XM_017012318.1:c.2106T>C XP_016867807.1:p.Tyr702=
NM_000441.2:c.2184T>C MANE Select NP_000432.1:p.Tyr728=