Canonical Allele Identifier: CA1522640519
Gene: SLC6A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1421821T= , CM000667.2:g.1421821T= GRCh38
NC_000005.9:g.1421936T= , CM000667.1:g.1421936T= GRCh37
NC_000005.8:g.1474936T= NCBI36
NG_015885.1:g.28608A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.792+55A= MANE Select ENSP00000270349.9:n.792+55A=
ENST00000270349.11:c.792+55A= ENSP00000270349.9:n.792+55A=
NM_001044.4:c.792+55A= NP_001035.1:n.792+55A=
NM_001044.5:c.792+55A= MANE Select NP_001035.1:n.792+55A=