Canonical Allele Identifier: CA14220736
Gene: SLC6A2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs168924

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.55655632A>G , CM000678.2:g.55655632A>G GRCh38
NC_000016.9:g.55689544A>G , CM000678.1:g.55689544A>G GRCh37
NC_000016.8:g.54247045A>G NCBI36
NG_016969.1:g.5003A>G

Transcript Alleles

HGVS Amino-acid change
NM_001172501.1:c.-589A>G VV NP_001165972.1:p.=
XM_011523295.1:c.-589A>G XP_011521597.1:p.=
XM_011523296.1:c.-589A>G XP_011521598.1:p.=
XM_011523297.1:c.-589A>G XP_011521599.1:p.=
XM_011523298.1:c.-589A>G XP_011521600.1:p.=
XR_933403.1:n.29A>G
XR_933603.1:n.21T>C
ENST00000568943.5:c.-589A>G ENSP00000457473.1:p.=