Canonical Allele Identifier: CA2708103628
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs2126356668

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1415636A>G , CM000667.2:g.1415636A>G GRCh38
NC_000005.9:g.1415751A>G , CM000667.1:g.1415751A>G GRCh37
NC_000005.8:g.1468751A>G NCBI36
NG_015885.1:g.34793T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1031+462T>C MANE Select ENSP00000270349.9:n.1031+462T>C
ENST00000270349.11:c.1031+462T>C ENSP00000270349.9:n.1031+462T>C
ENST00000511750.1:n.481+462T>C
NM_001044.4:c.1031+462T>C NP_001035.1:n.1031+462T>C
NM_001044.5:c.1031+462T>C MANE Select NP_001035.1:n.1031+462T>C