Canonical Allele Identifier: CA443020999
Gene: SLC6A3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.1416224G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1416109G>A , CM000667.2:g.1416109G>A GRCh38
NC_000005.9:g.1416224G>A , CM000667.1:g.1416224G>A GRCh37
NC_000005.8:g.1469224G>A NCBI36
NG_015885.1:g.34320C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1020C>T MANE Select ENSP00000270349.9:p.Asn340=
ENST00000270349.11:c.1020C>T ENSP00000270349.9:p.Asn340=
ENST00000511750.1:n.470C>T
NM_001044.4:c.1020C>T NP_001035.1:p.Asn340=
NM_001044.5:c.1020C>T MANE Select NP_001035.1:p.Asn340=
Search 100 bp 5'
Search 100 bp 3'