Canonical Allele Identifier: CA1522629321
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1756267658

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1415471T>C , CM000667.2:g.1415471T>C GRCh38
NC_000005.9:g.1415586T>C , CM000667.1:g.1415586T>C GRCh37
NC_000005.8:g.1468586T>C NCBI36
NG_015885.1:g.34958A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1031+627A>G MANE Select ENSP00000270349.9:n.1031+627A>G
ENST00000270349.11:c.1031+627A>G ENSP00000270349.9:n.1031+627A>G
ENST00000511750.1:n.481+627A>G
NM_001044.4:c.1031+627A>G NP_001035.1:n.1031+627A>G
NM_001044.5:c.1031+627A>G MANE Select NP_001035.1:n.1031+627A>G