Canonical Allele Identifier: CA1522628400
Gene: SLC6A3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1414761G= , CM000667.2:g.1414761G= GRCh38
NC_000005.9:g.1414876G= , CM000667.1:g.1414876G= GRCh37
NC_000005.8:g.1467876G= NCBI36
NG_015885.1:g.35668C=

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.1086C= MANE Select ENSP00000270349.9:p.Phe362=
ENST00000270349.11:c.1086C= ENSP00000270349.9:p.Phe362=
ENST00000511750.1:n.536C=
NM_001044.4:c.1086C= NP_001035.1:p.Phe362=
NM_001044.5:c.1086C= MANE Select NP_001035.1:p.Phe362=
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