Canonical Allele Identifier: CA1522641986
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1756522992
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1424014G>T , CM000667.2:g.1424014G>T GRCh38
NC_000005.9:g.1424129G>T , CM000667.1:g.1424129G>T GRCh37
NC_000005.8:g.1477129G>T NCBI36
NG_015885.1:g.26415C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.654-2000C>A MANE Select ENSP00000270349.9:n.654-2000C>A
ENST00000270349.11:c.654-2000C>A ENSP00000270349.9:n.654-2000C>A
NM_001044.4:c.654-2000C>A NP_001035.1:n.654-2000C>A
NM_001044.5:c.654-2000C>A MANE Select NP_001035.1:n.654-2000C>A
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