Canonical Allele Identifier: CA1522650169
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1756751126

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1433305C>T , CM000667.2:g.1433305C>T GRCh38
NC_000005.9:g.1433420C>T , CM000667.1:g.1433420C>T GRCh37
NC_000005.8:g.1486420C>T NCBI36
NG_015885.1:g.17124G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.419-607G>A MANE Select ENSP00000270349.9:n.419-607G>A
ENST00000270349.11:c.419-607G>A ENSP00000270349.9:n.419-607G>A
NM_001044.4:c.419-607G>A NP_001035.1:n.419-607G>A
NM_001044.5:c.419-607G>A MANE Select NP_001035.1:n.419-607G>A