Canonical Allele Identifier: CA2224349332
Gene: SLC12A3 HGNC NCBI

Linked Data

dbSNP Id: rs2055074212

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56870217_56870218insTGCTCCAGGTGAGGCCTG , CM000678.2:g.56870217_56870218insTGCTCCAGGTGAGGCCTG GRCh38
NC_000016.9:g.56904129_56904130insTGCTCCAGGTGAGGCCTG , CM000678.1:g.56904129_56904130insTGCTCCAGGTGAGGCCTG GRCh37
NC_000016.8:g.55461630_55461631insTGCTCCAGGTGAGGCCTG NCBI36
NG_009386.1:g.10011_10012insTGCTCCAGGTGAGGCCTG
NG_009386.2:g.10011_10012insTGCTCCAGGTGAGGCCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000563236.6:c.723_724insTGCTCCAGGTGAGGCCTG
ENST00000262502.5:c.720_721insTGCTCCAGGTGAGGCCTG
ENST00000438926.6:c.723_724insTGCTCCAGGTGAGGCCTG
ENST00000563236.5:c.723_724insTGCTCCAGGTGAGGCCTG
ENST00000566786.5:c.720_721insTGCTCCAGGTGAGGCCTG
NM_000339.2:c.723_724insTGCTCCAGGTGAGGCCTG
NM_001126107.1:c.720_721insTGCTCCAGGTGAGGCCTG
NM_001126108.1:c.723_724insTGCTCCAGGTGAGGCCTG
XM_005256119.1:c.720_721insTGCTCCAGGTGAGGCCTG
XM_005256119.2:c.720_721insTGCTCCAGGTGAGGCCTG
NM_000339.3:c.723_724insTGCTCCAGGTGAGGCCTG
NM_001126107.2:c.720_721insTGCTCCAGGTGAGGCCTG
NM_001126108.2:c.723_724insTGCTCCAGGTGAGGCCTG