Canonical Allele Identifier: CA443021012
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1343956648
gnomAD v2: 5-1416236-G-A
gnomAD v4: 5-1416121-G-A
MyVariant Identifiers: chr5:g.1416236G>A (hg19) chr5:g.1416121G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1416121G>A , CM000667.2:g.1416121G>A GRCh38
NC_000005.9:g.1416236G>A , CM000667.1:g.1416236G>A GRCh37
NC_000005.8:g.1469236G>A NCBI36
NG_015885.1:g.34308C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1008C>T MANE Select ENSP00000270349.9:p.Asn336=
ENST00000270349.11:c.1008C>T ENSP00000270349.9:p.Asn336=
ENST00000511750.1:n.458C>T
NM_001044.4:c.1008C>T NP_001035.1:p.Asn336=
NM_001044.5:c.1008C>T MANE Select NP_001035.1:p.Asn336=
Search 100 bp 5'
Search 100 bp 3'