Canonical Allele Identifier: CA396002372

Gene: SLC12A3

Linked Data

• MyVariant Identifiers: chr16:g.56938338T>G (hg19) ; chr16:g.56904426T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56904426T>G , CM000678.2:g.56904426T>G	GRCh38
NC_000016.9:g.56938338T>G , CM000678.1:g.56938338T>G	GRCh37
NC_000016.8:g.55495839T>G	NCBI36
NG_009386.1:g.44220T>G
NG_009386.2:g.44220T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563236.6:c.2888T>G MANE Select	ENSP00000456149.2:p.Val963Gly
ENST00000262502.5:c.2885T>G	ENSP00000262502.5:p.Val962Gly
ENST00000438926.6:c.2915T>G	ENSP00000402152.2:p.Val972Gly
ENST00000563236.5:c.2888T>G	ENSP00000456149.1:p.Val963Gly
ENST00000566786.5:c.2912T>G	ENSP00000457552.1:p.Val971Gly
ENST00000569002.1:n.319T>G
NM_000339.2:c.2915T>G	NP_000330.2:p.Val972Gly
NM_001126107.1:c.2912T>G	NP_001119579.1:p.Val971Gly
NM_001126108.1:c.2888T>G	NP_001119580.1:p.Val963Gly
XM_005256119.1:c.2885T>G	XP_005256176.1:p.Val962Gly
XM_005256119.2:c.2885T>G	XP_005256176.1:p.Val962Gly
NM_000339.3:c.2915T>G	NP_000330.3:p.Val972Gly
NM_001126107.2:c.2912T>G	NP_001119579.2:p.Val971Gly
NM_001126108.2:c.2888T>G MANE Select	NP_001119580.2:p.Val963Gly