Canonical Allele Identifier: CA1522634682
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1560902608
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1394914C>T , CM000667.2:g.1394914C>T GRCh38
NC_000005.9:g.1395029C>T , CM000667.1:g.1395029C>T GRCh37
NC_000005.8:g.1448029C>T NCBI36
NG_015885.1:g.55515G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.1840-156G>A MANE Select ENSP00000270349.9:n.1840-156G>A
ENST00000270349.11:c.1840-156G>A ENSP00000270349.9:n.1840-156G>A
ENST00000512002.2:n.221-156G>A
NM_001044.4:c.1840-156G>A NP_001035.1:n.1840-156G>A
NM_001044.5:c.1840-156G>A MANE Select NP_001035.1:n.1840-156G>A
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