Canonical Allele Identifier: CA359060894
Gene: SLC6A3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.1432735T>G (hg19) chr5:g.1432620T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1432620T>G , CM000667.2:g.1432620T>G GRCh38
NC_000005.9:g.1432735T>G , CM000667.1:g.1432735T>G GRCh37
NC_000005.8:g.1485735T>G NCBI36
NG_015885.1:g.17809A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.497A>C MANE Select ENSP00000270349.9:p.Tyr166Ser
ENST00000270349.11:c.497A>C ENSP00000270349.9:p.Tyr166Ser
NM_001044.4:c.497A>C NP_001035.1:p.Tyr166Ser
NM_001044.5:c.497A>C MANE Select NP_001035.1:p.Tyr166Ser
Search 100 bp 5'
Search 100 bp 3'