Canonical Allele Identifier: CA359060895
Gene: SLC6A3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.1432736A>T (hg19) chr5:g.1432621A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1432621A>T , CM000667.2:g.1432621A>T GRCh38
NC_000005.9:g.1432736A>T , CM000667.1:g.1432736A>T GRCh37
NC_000005.8:g.1485736A>T NCBI36
NG_015885.1:g.17808T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.496T>A MANE Select ENSP00000270349.9:p.Tyr166Asn
ENST00000270349.11:c.496T>A ENSP00000270349.9:p.Tyr166Asn
NM_001044.4:c.496T>A NP_001035.1:p.Tyr166Asn
NM_001044.5:c.496T>A MANE Select NP_001035.1:p.Tyr166Asn
Search 100 bp 5'
Search 100 bp 3'