Canonical Allele Identifier: CA1522655619
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1733753535

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1444536T>G , CM000667.2:g.1444536T>G GRCh38
NC_000005.9:g.1444651T>G , CM000667.1:g.1444651T>G GRCh37
NC_000005.8:g.1497651T>G NCBI36
NG_015885.1:g.5893A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.-46+812A>C MANE Select ENSP00000270349.9:n.-46+812A>C
ENST00000270349.11:c.-46+812A>C ENSP00000270349.9:n.-46+812A>C
NM_001044.4:c.-46+812A>C NP_001035.1:n.-46+812A>C
NM_001044.5:c.-46+812A>C MANE Select NP_001035.1:n.-46+812A>C