Canonical Allele Identifier: CA15887871
Gene: SLC6A2 HGNC NCBI

Linked Data

dbSNP Id: rs8049681

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55701438G>A , CM000678.2:g.55701438G>A GRCh38
NC_000016.9:g.55735350G>A , CM000678.1:g.55735350G>A GRCh37
NC_000016.8:g.54292851G>A NCBI36
NG_016969.1:g.50809G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000219833.13:c.1759-425G>A ENSP00000219833.8:n.1759-425G>A
ENST00000568943.6:c.1759-425G>A MANE Select ENSP00000457473.1:n.1759-425G>A
ENST00000574918.2:c.1624-425G>A ENSP00000460214.2:n.1624-425G>A
ENST00000682050.1:c.*458-425G>A ENSP00000508367.1:n.*458-425G>A
ENST00000219833.12:c.1759-425G>A ENSP00000219833.8:n.1759-425G>A
ENST00000379906.6:c.1759-425G>A ENSP00000369237.2:n.1759-425G>A
ENST00000414754.7:c.1591-425G>A ENSP00000394956.3:n.1591-425G>A
ENST00000561820.5:c.1758+1132G>A ENSP00000454439.1:n.1758+1132G>A
ENST00000566163.5:c.1624-425G>A ENSP00000456210.1:n.1624-425G>A
ENST00000567238.1:c.1444-425G>A ENSP00000457375.1:n.1444-425G>A
ENST00000568943.5:c.1759-425G>A ENSP00000457473.1:n.1759-425G>A
ENST00000574918.1:c.34-425G>A
NM_001043.3:c.1759-425G>A NP_001034.1:n.1759-425G>A
NM_001172501.1:c.1759-425G>A NP_001165972.1:n.1759-425G>A
NM_001172502.1:c.1444-425G>A NP_001165973.1:n.1444-425G>A
NM_001172504.1:c.1759-425G>A NP_001165975.1:n.1759-425G>A
XM_006721263.2:c.1759-425G>A XP_006721326.1:n.1759-425G>A
XM_011523295.1:c.1759-425G>A XP_011521597.1:n.1759-425G>A
XM_011523296.1:c.1624-425G>A XP_011521598.1:n.1624-425G>A
XM_011523297.1:c.1624-425G>A XP_011521599.1:n.1624-425G>A
XM_011523299.1:c.1036-425G>A XP_011521601.1:n.1036-425G>A
XM_011523300.1:c.1036-425G>A XP_011521602.1:n.1036-425G>A
XR_933403.1:n.2275-425G>A
XM_011523295.2:c.1759-425G>A XP_011521597.1:n.1759-425G>A
XM_011523296.2:c.1624-425G>A XP_011521598.1:n.1624-425G>A
XM_011523297.3:c.1624-425G>A XP_011521599.1:n.1624-425G>A
XM_011523299.2:c.1036-425G>A XP_011521601.1:n.1036-425G>A
XM_011523300.2:c.1036-425G>A XP_011521602.1:n.1036-425G>A
XR_933403.3:n.1951-425G>A
NM_001172501.2:c.1759-425G>A NP_001165972.1:n.1759-425G>A
NM_001172501.3:c.1759-425G>A MANE Select NP_001165972.1:n.1759-425G>A