Canonical Allele Identifier: CA1522640533
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1271181202

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1421854A>G , CM000667.2:g.1421854A>G GRCh38
NC_000005.9:g.1421969A>G , CM000667.1:g.1421969A>G GRCh37
NC_000005.8:g.1474969A>G NCBI36
NG_015885.1:g.28575T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.792+22T>C MANE Select ENSP00000270349.9:n.792+22T>C
ENST00000270349.11:c.792+22T>C ENSP00000270349.9:n.792+22T>C
NM_001044.4:c.792+22T>C NP_001035.1:n.792+22T>C
NM_001044.5:c.792+22T>C MANE Select NP_001035.1:n.792+22T>C