Canonical Allele Identifier: CA2708105619
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs2126395947

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1433266A>G , CM000667.2:g.1433266A>G GRCh38
NC_000005.9:g.1433381A>G , CM000667.1:g.1433381A>G GRCh37
NC_000005.8:g.1486381A>G NCBI36
NG_015885.1:g.17163T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.419-568T>C MANE Select ENSP00000270349.9:n.419-568T>C
ENST00000270349.11:c.419-568T>C ENSP00000270349.9:n.419-568T>C
NM_001044.4:c.419-568T>C NP_001035.1:n.419-568T>C
NM_001044.5:c.419-568T>C MANE Select NP_001035.1:n.419-568T>C