Canonical Allele Identifier: CA1522640532
Gene: SLC6A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1421854A= , CM000667.2:g.1421854A= GRCh38
NC_000005.9:g.1421969A= , CM000667.1:g.1421969A= GRCh37
NC_000005.8:g.1474969A= NCBI36
NG_015885.1:g.28575T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.792+22T= MANE Select ENSP00000270349.9:n.792+22T=
ENST00000270349.11:c.792+22T= ENSP00000270349.9:n.792+22T=
NM_001044.4:c.792+22T= NP_001035.1:n.792+22T=
NM_001044.5:c.792+22T= MANE Select NP_001035.1:n.792+22T=