Canonical Allele Identifier: CA1522626597
Gene: SLC6A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1414391C= , CM000667.2:g.1414391C= GRCh38
NC_000005.9:g.1414506C= , CM000667.1:g.1414506C= GRCh37
NC_000005.8:g.1467506C= NCBI36
NG_015885.1:g.36038G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1156+300G= MANE Select ENSP00000270349.9:n.1156+300G=
ENST00000270349.11:c.1156+300G= ENSP00000270349.9:n.1156+300G=
NM_001044.4:c.1156+300G= NP_001035.1:n.1156+300G=
NM_001044.5:c.1156+300G= MANE Select NP_001035.1:n.1156+300G=