Canonical Allele Identifier: CA359083179
Gene: SLC6A3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.1414877A>T (hg19) chr5:g.1414762A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1414762A>T , CM000667.2:g.1414762A>T GRCh38
NC_000005.9:g.1414877A>T , CM000667.1:g.1414877A>T GRCh37
NC_000005.8:g.1467877A>T NCBI36
NG_015885.1:g.35667T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.1085T>A MANE Select ENSP00000270349.9:p.Phe362Tyr
ENST00000270349.11:c.1085T>A ENSP00000270349.9:p.Phe362Tyr
ENST00000511750.1:n.535T>A
NM_001044.4:c.1085T>A NP_001035.1:p.Phe362Tyr
NM_001044.5:c.1085T>A MANE Select NP_001035.1:p.Phe362Tyr
Search 100 bp 5'
Search 100 bp 3'