Canonical Allele Identifier: CA1522649882
Gene: SLC6A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1432628C= , CM000667.2:g.1432628C= GRCh38
NC_000005.9:g.1432743C= , CM000667.1:g.1432743C= GRCh37
NC_000005.8:g.1485743C= NCBI36
NG_015885.1:g.17801G=

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.489G= MANE Select ENSP00000270349.9:p.Ala163=
ENST00000270349.11:c.489G= ENSP00000270349.9:p.Ala163=
NM_001044.4:c.489G= NP_001035.1:p.Ala163=
NM_001044.5:c.489G= MANE Select NP_001035.1:p.Ala163=