Canonical Allele Identifier: CA112963496
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs141057848
gnomAD v2: 5-1433449-T-TG
gnomAD v3: 5-1433334-T-TG
gnomAD v4: 5-1433334-T-TG
MyVariant Identifiers: chr5:g.1433449_1433450insG (hg19) chr5:g.1433334_1433335insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1433335dup , CM000667.2:g.1433335dup GRCh38
NC_000005.9:g.1433450dup , CM000667.1:g.1433450dup GRCh37
NC_000005.8:g.1486450dup NCBI36
NG_015885.1:g.17094dup

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.419-637dup MANE Select ENSP00000270349.9:n.419-637dup
ENST00000270349.11:c.419-637dup ENSP00000270349.9:n.419-637dup
NM_001044.4:c.419-637dup NP_001035.1:n.419-637dup
NM_001044.5:c.419-637dup MANE Select NP_001035.1:n.419-637dup
Search 100 bp 5'
Search 100 bp 3'