Canonical Allele Identifier: CA1522627404
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1756220688

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1414486G>C , CM000667.2:g.1414486G>C GRCh38
NC_000005.9:g.1414601G>C , CM000667.1:g.1414601G>C GRCh37
NC_000005.8:g.1467601G>C NCBI36
NG_015885.1:g.35943C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1156+205C>G MANE Select ENSP00000270349.9:n.1156+205C>G
ENST00000270349.11:c.1156+205C>G ENSP00000270349.9:n.1156+205C>G
NM_001044.4:c.1156+205C>G NP_001035.1:n.1156+205C>G
NM_001044.5:c.1156+205C>G MANE Select NP_001035.1:n.1156+205C>G