Canonical Allele Identifier: CA1522637726
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1756282272
gnomAD v4: 5-1416035-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1416035T>C , CM000667.2:g.1416035T>C GRCh38
NC_000005.9:g.1416150T>C , CM000667.1:g.1416150T>C GRCh37
NC_000005.8:g.1469150T>C NCBI36
NG_015885.1:g.34394A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.1031+63A>G MANE Select ENSP00000270349.9:n.1031+63A>G
ENST00000270349.11:c.1031+63A>G ENSP00000270349.9:n.1031+63A>G
ENST00000511750.1:n.481+63A>G
NM_001044.4:c.1031+63A>G NP_001035.1:n.1031+63A>G
NM_001044.5:c.1031+63A>G MANE Select NP_001035.1:n.1031+63A>G