Canonical Allele Identifier: CA2708103735
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs2126357462
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1415942C>A , CM000667.2:g.1415942C>A GRCh38
NC_000005.9:g.1416057C>A , CM000667.1:g.1416057C>A GRCh37
NC_000005.8:g.1469057C>A NCBI36
NG_015885.1:g.34487G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.1031+156G>T MANE Select ENSP00000270349.9:n.1031+156G>T
ENST00000270349.11:c.1031+156G>T ENSP00000270349.9:n.1031+156G>T
ENST00000511750.1:n.481+156G>T
NM_001044.4:c.1031+156G>T NP_001035.1:n.1031+156G>T
NM_001044.5:c.1031+156G>T MANE Select NP_001035.1:n.1031+156G>T
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