Canonical Allele Identifier: CA1522627998
Gene: SLC6A3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1414552C= , CM000667.2:g.1414552C= GRCh38
NC_000005.9:g.1414667C= , CM000667.1:g.1414667C= GRCh37
NC_000005.8:g.1467667C= NCBI36
NG_015885.1:g.35877G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1156+139G= MANE Select ENSP00000270349.9:n.1156+139G=
ENST00000270349.11:c.1156+139G= ENSP00000270349.9:n.1156+139G=
NM_001044.4:c.1156+139G= NP_001035.1:n.1156+139G=
NM_001044.5:c.1156+139G= MANE Select NP_001035.1:n.1156+139G=
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