Canonical Allele Identifier: CA804832279
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1212779139

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1423882T>G , CM000667.2:g.1423882T>G GRCh38
NC_000005.9:g.1423997T>G , CM000667.1:g.1423997T>G GRCh37
NC_000005.8:g.1476997T>G NCBI36
NG_015885.1:g.26547A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.654-1868A>C MANE Select ENSP00000270349.9:n.654-1868A>C
ENST00000270349.11:c.654-1868A>C ENSP00000270349.9:n.654-1868A>C
NM_001044.4:c.654-1868A>C NP_001035.1:n.654-1868A>C
NM_001044.5:c.654-1868A>C MANE Select NP_001035.1:n.654-1868A>C