Canonical Allele Identifier: CA1072522010
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs140094229
gnomAD v3: 5-1414398-T-TG
gnomAD v4: 5-1414398-T-TG

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1414405dup , CM000667.2:g.1414405dup GRCh38
NC_000005.9:g.1414520dup , CM000667.1:g.1414520dup GRCh37
NC_000005.8:g.1467520dup NCBI36
NG_015885.1:g.36030dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1156+292dup MANE Select ENSP00000270349.9:n.1156+292dup
ENST00000270349.11:c.1156+292dup ENSP00000270349.9:n.1156+292dup
NM_001044.4:c.1156+292dup NP_001035.1:n.1156+292dup
NM_001044.5:c.1156+292dup MANE Select NP_001035.1:n.1156+292dup