Canonical Allele Identifier: CA1522644000
Gene: SLC6A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1427967A= , CM000667.2:g.1427967A= GRCh38
NC_000005.9:g.1428082A= , CM000667.1:g.1428082A= GRCh37
NC_000005.8:g.1481082A= NCBI36
NG_015885.1:g.22462T=

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.653+4497T= MANE Select ENSP00000270349.9:n.653+4497T=
ENST00000270349.11:c.653+4497T= ENSP00000270349.9:n.653+4497T=
NM_001044.4:c.653+4497T= NP_001035.1:n.653+4497T=
NM_001044.5:c.653+4497T= MANE Select NP_001035.1:n.653+4497T=