Canonical Allele Identifier: CA1522644038
Gene: SLC6A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1428035G= , CM000667.2:g.1428035G= GRCh38
NC_000005.9:g.1428150G= , CM000667.1:g.1428150G= GRCh37
NC_000005.8:g.1481150G= NCBI36
NG_015885.1:g.22394C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.653+4429C= MANE Select ENSP00000270349.9:n.653+4429C=
ENST00000270349.11:c.653+4429C= ENSP00000270349.9:n.653+4429C=
NM_001044.4:c.653+4429C= NP_001035.1:n.653+4429C=
NM_001044.5:c.653+4429C= MANE Select NP_001035.1:n.653+4429C=