Canonical Allele Identifier: CA14266137
Gene: SLC6A2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1566652

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55697663G>T , CM000678.2:g.55697663G>T GRCh38
NC_000016.9:g.55731575G>T , CM000678.1:g.55731575G>T GRCh37
NC_000016.8:g.54289076G>T NCBI36
NG_016969.1:g.47034G>T

Transcript Alleles

HGVS Amino-acid change
NM_001043.3:c.1261-234G>T VV NP_001034.1:p.=
NM_001172501.1:c.1261-234G>T VV NP_001165972.1:p.=
NM_001172502.1:c.946-234G>T VV NP_001165973.1:p.=
NM_001172504.1:c.1261-234G>T VV NP_001165975.1:p.=
XM_006721263.2:c.1261-234G>T XP_006721326.1:p.=
XM_011523295.1:c.1261-234G>T XP_011521597.1:p.=
XM_011523296.1:c.1126-234G>T XP_011521598.1:p.=
XM_011523297.1:c.1126-234G>T XP_011521599.1:p.=
XM_011523298.1:c.1148-234G>T XP_011521600.1:p.=
XM_011523299.1:c.538-234G>T XP_011521601.1:p.=
XM_011523300.1:c.538-234G>T XP_011521602.1:p.=
XR_933403.1:n.1878-234G>T
XM_011523295.2:c.1261-234G>T
XM_011523296.2:c.1126-234G>T
XM_011523297.3:c.1126-234G>T
XM_011523298.2:c.1148-234G>T
XM_011523299.2:c.538-234G>T
XM_011523300.2:c.538-234G>T
XR_933403.3:n.1554-234G>T
ENST00000219833.12:c.1261-234G>T ENSP00000219833.8:p.=
ENST00000379906.6:c.1261-234G>T ENSP00000369237.2:p.=
ENST00000414754.7:c.1261-234G>T ENSP00000394956.3:p.=
ENST00000561820.5:c.1261-234G>T ENSP00000454439.1:p.=
ENST00000566163.5:c.1126-234G>T ENSP00000456210.1:p.=
ENST00000567238.1:c.946-234G>T ENSP00000457375.1:p.=
ENST00000568943.5:c.1261-234G>T ENSP00000457473.1:p.=