Canonical Allele Identifier: CA112968601
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs148890421

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1423800dup , CM000667.2:g.1423800dup GRCh38
NC_000005.9:g.1423915dup , CM000667.1:g.1423915dup GRCh37
NC_000005.8:g.1476915dup NCBI36
NG_015885.1:g.26629dup

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.654-1786dup MANE Select ENSP00000270349.9:n.654-1786dup
ENST00000270349.11:c.654-1786dup ENSP00000270349.9:n.654-1786dup
NM_001044.4:c.654-1786dup NP_001035.1:n.654-1786dup
NM_001044.5:c.654-1786dup MANE Select NP_001035.1:n.654-1786dup