Canonical Allele Identifier: CA2529795647
Gene: SLC6A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55656487T>C , CM000678.2:g.55656487T>C GRCh38
NC_000016.9:g.55690399T>C , CM000678.1:g.55690399T>C GRCh37
NC_000016.8:g.54247900T>C NCBI36
NG_016969.1:g.5858T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000219833.13:c.-208T>C ENSP00000219833.8:n.-208T>C
ENST00000568943.6:c.-51-157T>C MANE Select ENSP00000457473.1:n.-51-157T>C
ENST00000574918.2:c.-52+135T>C ENSP00000460214.2:n.-52+135T>C
ENST00000682050.1:c.-52+135T>C ENSP00000508367.1:n.-52+135T>C
ENST00000379906.6:c.-208T>C ENSP00000369237.2:n.-208T>C
ENST00000414754.7:c.-51-157T>C ENSP00000394956.3:n.-51-157T>C
ENST00000568529.6:c.-51-157T>C ENSP00000456377.2:n.-51-157T>C
ENST00000568655.5:c.-52+135T>C ENSP00000454603.1:n.-52+135T>C
ENST00000568943.5:c.-51-157T>C ENSP00000457473.1:n.-51-157T>C
NM_001043.3:c.-208T>C NP_001034.1:n.-208T>C
NM_001172501.1:c.-51-157T>C NP_001165972.1:n.-51-157T>C
XM_006721263.2:c.-52+135T>C XP_006721326.1:n.-52+135T>C
XM_011523295.1:c.-51-157T>C XP_011521597.1:n.-51-157T>C
XM_011523296.1:c.-51-157T>C XP_011521598.1:n.-51-157T>C
XM_011523297.1:c.-51-157T>C XP_011521599.1:n.-51-157T>C
XM_011523298.1:c.-51-157T>C XP_011521600.1:n.-51-157T>C
XR_933403.1:n.567-157T>C
XM_011523295.2:c.-51-157T>C XP_011521597.1:n.-51-157T>C
XM_011523296.2:c.-51-157T>C XP_011521598.1:n.-51-157T>C
XM_011523297.3:c.-51-157T>C XP_011521599.1:n.-51-157T>C
XM_011523298.2:c.-51-157T>C XP_011521600.1:n.-51-157T>C
XR_933403.3:n.243-157T>C
NM_001172501.2:c.-51-157T>C NP_001165972.1:n.-51-157T>C
NM_001172501.3:c.-51-157T>C MANE Select NP_001165972.1:n.-51-157T>C