Canonical Allele Identifier: CA1522650162
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1756750831

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1433290A>G , CM000667.2:g.1433290A>G GRCh38
NC_000005.9:g.1433405A>G , CM000667.1:g.1433405A>G GRCh37
NC_000005.8:g.1486405A>G NCBI36
NG_015885.1:g.17139T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.419-592T>C MANE Select ENSP00000270349.9:n.419-592T>C
ENST00000270349.11:c.419-592T>C ENSP00000270349.9:n.419-592T>C
NM_001044.4:c.419-592T>C NP_001035.1:n.419-592T>C
NM_001044.5:c.419-592T>C MANE Select NP_001035.1:n.419-592T>C