Canonical Allele Identifier: CA112963503
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs995991998

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1433372G>C , CM000667.2:g.1433372G>C GRCh38
NC_000005.9:g.1433487G>C , CM000667.1:g.1433487G>C GRCh37
NC_000005.8:g.1486487G>C NCBI36
NG_015885.1:g.17057C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.419-674C>G MANE Select ENSP00000270349.9:n.419-674C>G
ENST00000270349.11:c.419-674C>G ENSP00000270349.9:n.419-674C>G
NM_001044.4:c.419-674C>G NP_001035.1:n.419-674C>G
NM_001044.5:c.419-674C>G MANE Select NP_001035.1:n.419-674C>G