Canonical Allele Identifier: CA557566099
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1756226735
gnomAD v2: 5-1414633-G-GGC
gnomAD v3: 5-1414518-G-GGC
gnomAD v4: 5-1414518-G-GGC
MyVariant Identifiers: chr5:g.1414633_1414634insGC (hg19) chr5:g.1414518_1414519insGC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1414518_1414519insGC , CM000667.2:g.1414518_1414519insGC GRCh38
NC_000005.9:g.1414633_1414634insGC , CM000667.1:g.1414633_1414634insGC GRCh37
NC_000005.8:g.1467633_1467634insGC NCBI36
NG_015885.1:g.35910_35911insGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1156+172_1156+173insGC MANE Select ENSP00000270349.9:n.1156+172_1156+173insGC
ENST00000270349.11:c.1156+172_1156+173insGC ENSP00000270349.9:n.1156+172_1156+173insGC
NM_001044.4:c.1156+172_1156+173insGC NP_001035.1:n.1156+172_1156+173insGC
NM_001044.5:c.1156+172_1156+173insGC MANE Select NP_001035.1:n.1156+172_1156+173insGC
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