Canonical Allele Identifier: CA112964309
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs763019310
MyVariant Identifiers: chr5:g.1416213C>T (hg19) chr5:g.1416098C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1416098C>T , CM000667.2:g.1416098C>T GRCh38
NC_000005.9:g.1416213C>T , CM000667.1:g.1416213C>T GRCh37
NC_000005.8:g.1469213C>T NCBI36
NG_015885.1:g.34331G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1031G>A MANE Select ENSP00000270349.9:p.Arg344Lys
ENST00000270349.11:c.1031G>A ENSP00000270349.9:p.Arg344Lys
ENST00000511750.1:n.481G>A
NM_001044.4:c.1031G>A NP_001035.1:p.Arg344Lys
NM_001044.5:c.1031G>A MANE Select NP_001035.1:p.Arg344Lys
Search 100 bp 5'
Search 100 bp 3'