Canonical Allele Identifier: CA804997483
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1277537508
gnomAD v3: 5-1443621-C-CT
gnomAD v4: 5-1443621-C-CT
MyVariant Identifiers: chr5:g.1443736_1443737insT (hg19) chr5:g.1443621_1443622insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1443623dup , CM000667.2:g.1443623dup GRCh38
NC_000005.9:g.1443738dup , CM000667.1:g.1443738dup GRCh37
NC_000005.8:g.1496738dup NCBI36
NG_015885.1:g.6807dup

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.-45-380dup MANE Select ENSP00000270349.9:n.-45-380dup
ENST00000270349.11:c.-45-380dup ENSP00000270349.9:n.-45-380dup
NM_001044.4:c.-45-380dup NP_001035.1:n.-45-380dup
NM_001044.5:c.-45-380dup MANE Select NP_001035.1:n.-45-380dup
Search 100 bp 5'
Search 100 bp 3'