Canonical Allele Identifier: CA804914012
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1230109012
gnomAD v3: 5-1433215-A-AATC
gnomAD v4: 5-1433215-A-AATC
MyVariant Identifiers: chr5:g.1433330_1433331insATC (hg19) chr5:g.1433215_1433216insATC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1433219_1433221dup , CM000667.2:g.1433219_1433221dup GRCh38
NC_000005.9:g.1433334_1433336dup , CM000667.1:g.1433334_1433336dup GRCh37
NC_000005.8:g.1486334_1486336dup NCBI36
NG_015885.1:g.17211_17213dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.419-520_419-518dup MANE Select ENSP00000270349.9:n.419-520_419-518dup
ENST00000270349.11:c.419-520_419-518dup ENSP00000270349.9:n.419-520_419-518dup
NM_001044.4:c.419-520_419-518dup NP_001035.1:n.419-520_419-518dup
NM_001044.5:c.419-520_419-518dup MANE Select NP_001035.1:n.419-520_419-518dup
Search 100 bp 5'
Search 100 bp 3'