Canonical Allele Identifier: CA1522644254
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1756617089

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1428303G>T , CM000667.2:g.1428303G>T GRCh38
NC_000005.9:g.1428418G>T , CM000667.1:g.1428418G>T GRCh37
NC_000005.8:g.1481418G>T NCBI36
NG_015885.1:g.22126C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.653+4161C>A MANE Select ENSP00000270349.9:n.653+4161C>A
ENST00000270349.11:c.653+4161C>A ENSP00000270349.9:n.653+4161C>A
NM_001044.4:c.653+4161C>A NP_001035.1:n.653+4161C>A
NM_001044.5:c.653+4161C>A MANE Select NP_001035.1:n.653+4161C>A