Canonical Allele Identifier: CA3186291
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs750078703
gnomAD v2: 5-1422114-G-A
gnomAD v4: 5-1421999-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1421999G>A , CM000667.2:g.1421999G>A GRCh38
NC_000005.9:g.1422114G>A , CM000667.1:g.1422114G>A GRCh37
NC_000005.8:g.1475114G>A NCBI36
NG_015885.1:g.28430C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.669C>T MANE Select ENSP00000270349.9:p.His223=
ENST00000270349.11:c.669C>T ENSP00000270349.9:p.His223=
NM_001044.4:c.669C>T NP_001035.1:p.His223=
NM_001044.5:c.669C>T MANE Select NP_001035.1:p.His223=