Canonical Allele Identifier: CA8061703

Gene: SLC6A2

Linked Data

• dbSNP Id: rs762381614
• ExAC: 16:55730249 A / G
• gnomAD v2: 16-55730249-A-G
• gnomAD v4: 16-55696337-A-G
• MyVariant Identifiers: chr16:g.55730249A>G (hg19) ; chr16:g.55696337A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.55696337A>G , CM000678.2:g.55696337A>G	GRCh38
NC_000016.9:g.55730249A>G , CM000678.1:g.55730249A>G	GRCh37
NC_000016.8:g.54287750A>G	NCBI36
NG_016969.1:g.45708A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219833.13:c.1260A>G	ENSP00000219833.8:p.Ser420=
ENST00000568943.6:c.1260A>G MANE Select	ENSP00000457473.1:p.Ser420=
ENST00000574918.2:c.1125A>G	ENSP00000460214.2:p.Ser375=
ENST00000682050.1:c.1012+935A>G	ENSP00000508367.1:n.1012+935A>G
ENST00000219833.12:c.1260A>G	ENSP00000219833.8:p.Ser420=
ENST00000379906.6:c.1260A>G	ENSP00000369237.2:p.Ser420=
ENST00000414754.7:c.1260A>G	ENSP00000394956.3:p.Ser420=
ENST00000561820.5:c.1260A>G	ENSP00000454439.1:p.Ser420=
ENST00000566163.5:c.1125A>G	ENSP00000456210.1:p.Ser375=
ENST00000567238.1:c.945A>G	ENSP00000457375.1:p.Ser315=
ENST00000568943.5:c.1260A>G	ENSP00000457473.1:p.Ser420=
NM_001043.3:c.1260A>G	NP_001034.1:p.Ser420=
NM_001172501.1:c.1260A>G	NP_001165972.1:p.Ser420=
NM_001172502.1:c.945A>G	NP_001165973.1:p.Ser315=
NM_001172504.1:c.1260A>G	NP_001165975.1:p.Ser420=
XM_006721263.2:c.1260A>G	XP_006721326.1:p.Ser420=
XM_011523295.1:c.1260A>G	XP_011521597.1:p.Ser420=
XM_011523296.1:c.1125A>G	XP_011521598.1:p.Ser375=
XM_011523297.1:c.1125A>G	XP_011521599.1:p.Ser375=
XM_011523298.1:c.1147+935A>G	XP_011521600.1:n.1147+935A>G
XM_011523299.1:c.537A>G	XP_011521601.1:p.Ser179=
XM_011523300.1:c.537A>G	XP_011521602.1:p.Ser179=
XR_933403.1:n.1877A>G
XM_011523295.2:c.1260A>G	XP_011521597.1:p.Ser420=
XM_011523296.2:c.1125A>G	XP_011521598.1:p.Ser375=
XM_011523297.3:c.1125A>G	XP_011521599.1:p.Ser375=
XM_011523298.2:c.1147+935A>G	XP_011521600.1:n.1147+935A>G
XM_011523299.2:c.537A>G	XP_011521601.1:p.Ser179=
XM_011523300.2:c.537A>G	XP_011521602.1:p.Ser179=
XR_933403.3:n.1553A>G
NM_001172501.2:c.1260A>G	NP_001165972.1:p.Ser420=
NM_001172501.3:c.1260A>G MANE Select	NP_001165972.1:p.Ser420=