Canonical Allele Identifier: CA804914025
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1409173871

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1433329A>C , CM000667.2:g.1433329A>C GRCh38
NC_000005.9:g.1433444A>C , CM000667.1:g.1433444A>C GRCh37
NC_000005.8:g.1486444A>C NCBI36
NG_015885.1:g.17100T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.419-631T>G MANE Select ENSP00000270349.9:n.419-631T>G
ENST00000270349.11:c.419-631T>G ENSP00000270349.9:n.419-631T>G
NM_001044.4:c.419-631T>G NP_001035.1:n.419-631T>G
NM_001044.5:c.419-631T>G MANE Select NP_001035.1:n.419-631T>G