Canonical Allele Identifier: CA112963143
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs549470632
gnomAD v2: 5-1414590-T-TG
gnomAD v3: 5-1414475-T-TG
gnomAD v4: 5-1414475-T-TG
MyVariant Identifiers: chr5:g.1414591_1414592insG (hg19) chr5:g.1414590_1414591insG (hg19) chr5:g.1414476_1414477insG (hg38) chr5:g.1414475_1414476insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1414481dup , CM000667.2:g.1414481dup GRCh38
NC_000005.9:g.1414596dup , CM000667.1:g.1414596dup GRCh37
NC_000005.8:g.1467596dup NCBI36
NG_015885.1:g.35953dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1156+215dup MANE Select ENSP00000270349.9:n.1156+215dup
ENST00000270349.11:c.1156+215dup ENSP00000270349.9:n.1156+215dup
NM_001044.4:c.1156+215dup NP_001035.1:n.1156+215dup
NM_001044.5:c.1156+215dup MANE Select NP_001035.1:n.1156+215dup
Search 100 bp 5'
Search 100 bp 3'