Canonical Allele Identifier: CA804997731
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1416768942

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1444247A>C , CM000667.2:g.1444247A>C GRCh38
NC_000005.9:g.1444362A>C , CM000667.1:g.1444362A>C GRCh37
NC_000005.8:g.1497362A>C NCBI36
NG_015885.1:g.6182T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.-45-1005T>G MANE Select ENSP00000270349.9:n.-45-1005T>G
ENST00000270349.11:c.-45-1005T>G ENSP00000270349.9:n.-45-1005T>G
NM_001044.4:c.-45-1005T>G NP_001035.1:n.-45-1005T>G
NM_001044.5:c.-45-1005T>G MANE Select NP_001035.1:n.-45-1005T>G