Canonical Allele Identifier: CA112954003
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs891566029
MyVariant Identifiers: chr5:g.1394442A>G (hg19) chr5:g.1394327A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1394327A>G , CM000667.2:g.1394327A>G GRCh38
NC_000005.9:g.1394442A>G , CM000667.1:g.1394442A>G GRCh37
NC_000005.8:g.1447442A>G NCBI36
NG_015885.1:g.56102T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.*408T>C MANE Select ENSP00000270349.9:n.*408T>C
ENST00000270349.11:c.*408T>C ENSP00000270349.9:n.*408T>C
ENST00000512002.2:n.652T>C
NM_001044.4:c.*408T>C NP_001035.1:n.*408T>C
NM_001044.5:c.*408T>C MANE Select NP_001035.1:n.*408T>C
Search 100 bp 5'
Search 100 bp 3'