Canonical Allele Identifier: CA2633372567

Gene: SLC12A3

Linked Data

• gnomAD v4: 16-56870802-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56870802T>G , CM000678.2:g.56870802T>G	GRCh38
NC_000016.9:g.56904714T>G , CM000678.1:g.56904714T>G	GRCh37
NC_000016.8:g.55462215T>G	NCBI36
NG_009386.1:g.10596T>G
NG_009386.2:g.10596T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563236.6:c.852+66T>G MANE Select	ENSP00000456149.2:n.852+66T>G
ENST00000262502.5:c.849+66T>G	ENSP00000262502.5:n.849+66T>G
ENST00000438926.6:c.852+66T>G	ENSP00000402152.2:n.852+66T>G
ENST00000563236.5:c.852+66T>G	ENSP00000456149.1:n.852+66T>G
ENST00000566786.5:c.849+66T>G	ENSP00000457552.1:n.849+66T>G
NM_000339.2:c.852+66T>G	NP_000330.2:n.852+66T>G
NM_001126107.1:c.849+66T>G	NP_001119579.1:n.849+66T>G
NM_001126108.1:c.852+66T>G	NP_001119580.1:n.852+66T>G
XM_005256119.1:c.849+66T>G	XP_005256176.1:n.849+66T>G
XM_005256119.2:c.849+66T>G	XP_005256176.1:n.849+66T>G
NM_000339.3:c.852+66T>G	NP_000330.3:n.852+66T>G
NM_001126107.2:c.849+66T>G	NP_001119579.2:n.849+66T>G
NM_001126108.2:c.852+66T>G MANE Select	NP_001119580.2:n.852+66T>G