Canonical Allele Identifier: CA112963076
Gene: SLC6A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1206907
ClinVar RCV Id: RCV001574711
dbSNP Id: rs111302651
gnomAD v2: 5-1414507-A-G
gnomAD v3: 5-1414392-A-G
gnomAD v4: 5-1414392-A-G
MyVariant Identifiers: chr5:g.1414507A>G (hg19) chr5:g.1414507_1414540delinsGCTGGGTGGGGGGGCCTGGAGGGGCAGGGCGGAG (hg19) chr5:g.1414392A>G (hg38) chr5:g.1414392_1414425delinsGCTGGGTGGGGGGGCCTGGAGGGGCAGGGCGGAG (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1414392A>G , CM000667.2:g.1414392A>G GRCh38
NC_000005.9:g.1414507A>G , CM000667.1:g.1414507A>G GRCh37
NC_000005.8:g.1467507A>G NCBI36
NG_015885.1:g.36037T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1156+299T>C MANE Select ENSP00000270349.9:n.1156+299T>C
ENST00000270349.11:c.1156+299T>C ENSP00000270349.9:n.1156+299T>C
NM_001044.4:c.1156+299T>C NP_001035.1:n.1156+299T>C
NM_001044.5:c.1156+299T>C MANE Select NP_001035.1:n.1156+299T>C
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