Canonical Allele Identifier: CA804914017
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1293981611
gnomAD v3: 5-1433231-C-A
gnomAD v4: 5-1433231-C-A
MyVariant Identifiers: chr5:g.1433346C>A (hg19) chr5:g.1433231C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1433231C>A , CM000667.2:g.1433231C>A GRCh38
NC_000005.9:g.1433346C>A , CM000667.1:g.1433346C>A GRCh37
NC_000005.8:g.1486346C>A NCBI36
NG_015885.1:g.17198G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.419-533G>T MANE Select ENSP00000270349.9:n.419-533G>T
ENST00000270349.11:c.419-533G>T ENSP00000270349.9:n.419-533G>T
NM_001044.4:c.419-533G>T NP_001035.1:n.419-533G>T
NM_001044.5:c.419-533G>T MANE Select NP_001035.1:n.419-533G>T
Search 100 bp 5'
Search 100 bp 3'