Canonical Allele Identifier: CA1522649916
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1756734477

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1432717C>A , CM000667.2:g.1432717C>A GRCh38
NC_000005.9:g.1432832C>A , CM000667.1:g.1432832C>A GRCh37
NC_000005.8:g.1485832C>A NCBI36
NG_015885.1:g.17712G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.419-19G>T MANE Select ENSP00000270349.9:n.419-19G>T
ENST00000270349.11:c.419-19G>T ENSP00000270349.9:n.419-19G>T
NM_001044.4:c.419-19G>T NP_001035.1:n.419-19G>T
NM_001044.5:c.419-19G>T MANE Select NP_001035.1:n.419-19G>T