Canonical Allele Identifier: CA2708111177
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs2126370801

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1421828T>C , CM000667.2:g.1421828T>C GRCh38
NC_000005.9:g.1421943T>C , CM000667.1:g.1421943T>C GRCh37
NC_000005.8:g.1474943T>C NCBI36
NG_015885.1:g.28601A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.792+48A>G MANE Select ENSP00000270349.9:n.792+48A>G
ENST00000270349.11:c.792+48A>G ENSP00000270349.9:n.792+48A>G
NM_001044.4:c.792+48A>G NP_001035.1:n.792+48A>G
NM_001044.5:c.792+48A>G MANE Select NP_001035.1:n.792+48A>G