Canonical Allele Identifier: CA359083829
Gene: SLC6A3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.1416229T>A (hg19) chr5:g.1416114T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1416114T>A , CM000667.2:g.1416114T>A GRCh38
NC_000005.9:g.1416229T>A , CM000667.1:g.1416229T>A GRCh37
NC_000005.8:g.1469229T>A NCBI36
NG_015885.1:g.34315A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.1015A>T MANE Select ENSP00000270349.9:p.Thr339Ser
ENST00000270349.11:c.1015A>T ENSP00000270349.9:p.Thr339Ser
ENST00000511750.1:n.465A>T
NM_001044.4:c.1015A>T NP_001035.1:p.Thr339Ser
NM_001044.5:c.1015A>T MANE Select NP_001035.1:p.Thr339Ser
Search 100 bp 5'
Search 100 bp 3'