Canonical Allele Identifier: CA112963517
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs760588470
gnomAD v2: 5-1433546-CCA-C
gnomAD v3: 5-1433431-CCA-C
gnomAD v4: 5-1433431-CCA-C
MyVariant Identifiers: chr5:g.1433547_1433548del (hg19) chr5:g.1433432_1433433del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1433433_1433434del , CM000667.2:g.1433433_1433434del GRCh38
NC_000005.9:g.1433548_1433549del , CM000667.1:g.1433548_1433549del GRCh37
NC_000005.8:g.1486548_1486549del NCBI36
NG_015885.1:g.16996_16997del

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.419-735_419-734del MANE Select ENSP00000270349.9:n.419-735_419-734del
ENST00000270349.11:c.419-735_419-734del ENSP00000270349.9:n.419-735_419-734del
NM_001044.4:c.419-735_419-734del NP_001035.1:n.419-735_419-734del
NM_001044.5:c.419-735_419-734del MANE Select NP_001035.1:n.419-735_419-734del
Search 100 bp 5'
Search 100 bp 3'