Canonical Allele Identifier: CA2708103554
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs2126417039

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1443659T>C , CM000667.2:g.1443659T>C GRCh38
NC_000005.9:g.1443774T>C , CM000667.1:g.1443774T>C GRCh37
NC_000005.8:g.1496774T>C NCBI36
NG_015885.1:g.6770A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.-45-417A>G MANE Select ENSP00000270349.9:n.-45-417A>G
ENST00000270349.11:c.-45-417A>G ENSP00000270349.9:n.-45-417A>G
NM_001044.4:c.-45-417A>G NP_001035.1:n.-45-417A>G
NM_001044.5:c.-45-417A>G MANE Select NP_001035.1:n.-45-417A>G