Canonical Allele Identifier: CA804913627
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1398018992
MyVariant Identifiers: chr5:g.1431136C>T (hg19) chr5:g.1431021C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1431021C>T , CM000667.2:g.1431021C>T GRCh38
NC_000005.9:g.1431136C>T , CM000667.1:g.1431136C>T GRCh37
NC_000005.8:g.1484136C>T NCBI36
NG_015885.1:g.19408G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.653+1443G>A MANE Select ENSP00000270349.9:n.653+1443G>A
ENST00000270349.11:c.653+1443G>A ENSP00000270349.9:n.653+1443G>A
NM_001044.4:c.653+1443G>A NP_001035.1:n.653+1443G>A
NM_001044.5:c.653+1443G>A MANE Select NP_001035.1:n.653+1443G>A
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