Canonical Allele Identifier: CA1522649038
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1579721563
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1430890A>C , CM000667.2:g.1430890A>C GRCh38
NC_000005.9:g.1431005A>C , CM000667.1:g.1431005A>C GRCh37
NC_000005.8:g.1484005A>C NCBI36
NG_015885.1:g.19539T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.653+1574T>G MANE Select ENSP00000270349.9:n.653+1574T>G
ENST00000270349.11:c.653+1574T>G ENSP00000270349.9:n.653+1574T>G
NM_001044.4:c.653+1574T>G NP_001035.1:n.653+1574T>G
NM_001044.5:c.653+1574T>G MANE Select NP_001035.1:n.653+1574T>G
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