Canonical Allele Identifier: CA112963421
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs746822034
MyVariant Identifiers: chr5:g.1433291del (hg19) chr5:g.1433176del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1433176del , CM000667.2:g.1433176del GRCh38
NC_000005.9:g.1433291del , CM000667.1:g.1433291del GRCh37
NC_000005.8:g.1486291del NCBI36
NG_015885.1:g.17253del

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.419-478del MANE Select ENSP00000270349.9:n.419-478del
ENST00000270349.11:c.419-478del ENSP00000270349.9:n.419-478del
NM_001044.4:c.419-478del NP_001035.1:n.419-478del
NM_001044.5:c.419-478del MANE Select NP_001035.1:n.419-478del
Search 100 bp 5'
Search 100 bp 3'