Canonical Allele Identifier: CA1522623632
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1756108271

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1411011C>T , CM000667.2:g.1411011C>T GRCh38
NC_000005.9:g.1411126C>T , CM000667.1:g.1411126C>T GRCh37
NC_000005.8:g.1464126C>T NCBI36
NG_015885.1:g.39418G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1269+232G>A MANE Select ENSP00000270349.9:n.1269+232G>A
ENST00000270349.11:c.1269+232G>A ENSP00000270349.9:n.1269+232G>A
NM_001044.4:c.1269+232G>A NP_001035.1:n.1269+232G>A
NM_001044.5:c.1269+232G>A MANE Select NP_001035.1:n.1269+232G>A