Canonical Allele Identifier: CA443020705
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1481746800
gnomAD v3: 5-1414481-G-GCC
gnomAD v4: 5-1414481-G-GCC
MyVariant Identifiers: chr5:g.1414596_1414597insCC (hg19) chr5:g.1414481_1414482insCC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1414482_1414483dup , CM000667.2:g.1414482_1414483dup GRCh38
NC_000005.9:g.1414597_1414598dup , CM000667.1:g.1414597_1414598dup GRCh37
NC_000005.8:g.1467597_1467598dup NCBI36
NG_015885.1:g.35946_35947dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1156+208_1156+209dup MANE Select ENSP00000270349.9:n.1156+208_1156+209dup
ENST00000270349.11:c.1156+208_1156+209dup ENSP00000270349.9:n.1156+208_1156+209dup
NM_001044.4:c.1156+208_1156+209dup NP_001035.1:n.1156+208_1156+209dup
NM_001044.5:c.1156+208_1156+209dup MANE Select NP_001035.1:n.1156+208_1156+209dup
Search 100 bp 5'
Search 100 bp 3'