Canonical Allele Identifier: CA112968629
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs900978086
MyVariant Identifiers: chr5:g.1423958A>G (hg19) chr5:g.1423843A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1423843A>G , CM000667.2:g.1423843A>G GRCh38
NC_000005.9:g.1423958A>G , CM000667.1:g.1423958A>G GRCh37
NC_000005.8:g.1476958A>G NCBI36
NG_015885.1:g.26586T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.654-1829T>C MANE Select ENSP00000270349.9:n.654-1829T>C
ENST00000270349.11:c.654-1829T>C ENSP00000270349.9:n.654-1829T>C
NM_001044.4:c.654-1829T>C NP_001035.1:n.654-1829T>C
NM_001044.5:c.654-1829T>C MANE Select NP_001035.1:n.654-1829T>C
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