Canonical Allele Identifier: CA1522637722
Gene: SLC6A3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1416027C= , CM000667.2:g.1416027C= GRCh38
NC_000005.9:g.1416142C= , CM000667.1:g.1416142C= GRCh37
NC_000005.8:g.1469142C= NCBI36
NG_015885.1:g.34402G=

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.1031+71G= MANE Select ENSP00000270349.9:n.1031+71G=
ENST00000270349.11:c.1031+71G= ENSP00000270349.9:n.1031+71G=
ENST00000511750.1:n.481+71G=
NM_001044.4:c.1031+71G= NP_001035.1:n.1031+71G=
NM_001044.5:c.1031+71G= MANE Select NP_001035.1:n.1031+71G=
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