Canonical Allele Identifier: CA1522655625
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs999775804

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1444550C>G , CM000667.2:g.1444550C>G GRCh38
NC_000005.9:g.1444665C>G , CM000667.1:g.1444665C>G GRCh37
NC_000005.8:g.1497665C>G NCBI36
NG_015885.1:g.5879G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.-46+798G>C MANE Select ENSP00000270349.9:n.-46+798G>C
ENST00000270349.11:c.-46+798G>C ENSP00000270349.9:n.-46+798G>C
NM_001044.4:c.-46+798G>C NP_001035.1:n.-46+798G>C
NM_001044.5:c.-46+798G>C MANE Select NP_001035.1:n.-46+798G>C