Canonical Allele Identifier: CA1522628029
Gene: SLC6A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1414572T= , CM000667.2:g.1414572T= GRCh38
NC_000005.9:g.1414687T= , CM000667.1:g.1414687T= GRCh37
NC_000005.8:g.1467687T= NCBI36
NG_015885.1:g.35857A=

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.1156+119A= MANE Select ENSP00000270349.9:n.1156+119A=
ENST00000270349.11:c.1156+119A= ENSP00000270349.9:n.1156+119A=
NM_001044.4:c.1156+119A= NP_001035.1:n.1156+119A=
NM_001044.5:c.1156+119A= MANE Select NP_001035.1:n.1156+119A=