Canonical Allele Identifier: CA112963434
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1014317453

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1433195G>C , CM000667.2:g.1433195G>C GRCh38
NC_000005.9:g.1433310G>C , CM000667.1:g.1433310G>C GRCh37
NC_000005.8:g.1486310G>C NCBI36
NG_015885.1:g.17234C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.419-497C>G MANE Select ENSP00000270349.9:n.419-497C>G
ENST00000270349.11:c.419-497C>G ENSP00000270349.9:n.419-497C>G
NM_001044.4:c.419-497C>G NP_001035.1:n.419-497C>G
NM_001044.5:c.419-497C>G MANE Select NP_001035.1:n.419-497C>G