Canonical Allele Identifier: CA8069450
Gene: SLC12A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 319902
dbSNP Id: rs142199602

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56879592C>T , CM000678.2:g.56879592C>T GRCh38
NC_000016.9:g.56913504C>T , CM000678.1:g.56913504C>T GRCh37
NC_000016.8:g.55471005C>T NCBI36
NG_009386.1:g.19386C>T
NG_009386.2:g.19386C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000563236.6:c.1386C>T MANE Select ENSP00000456149.2:p.Phe462=
ENST00000262502.5:c.1383C>T ENSP00000262502.5:p.Phe461=
ENST00000438926.6:c.1386C>T ENSP00000402152.2:p.Phe462=
ENST00000563236.5:c.1386C>T ENSP00000456149.1:p.Phe462=
ENST00000566786.5:c.1383C>T ENSP00000457552.1:p.Phe461=
NM_000339.2:c.1386C>T NP_000330.2:p.Phe462=
NM_001126107.1:c.1383C>T NP_001119579.1:p.Phe461=
NM_001126108.1:c.1386C>T NP_001119580.1:p.Phe462=
XM_005256119.1:c.1383C>T XP_005256176.1:p.Phe461=
XM_005256119.2:c.1383C>T XP_005256176.1:p.Phe461=
NM_000339.3:c.1386C>T NP_000330.3:p.Phe462=
NM_001126107.2:c.1383C>T NP_001119579.2:p.Phe461=
NM_001126108.2:c.1386C>T MANE Select NP_001119580.2:p.Phe462=