Canonical Allele Identifier: CA443020984
Gene: SLC6A3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.1416214T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1416099T>G , CM000667.2:g.1416099T>G GRCh38
NC_000005.9:g.1416214T>G , CM000667.1:g.1416214T>G GRCh37
NC_000005.8:g.1469214T>G NCBI36
NG_015885.1:g.34330A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1030A>C MANE Select ENSP00000270349.9:p.Arg344=
ENST00000270349.11:c.1030A>C ENSP00000270349.9:p.Arg344=
ENST00000511750.1:n.480A>C
NM_001044.4:c.1030A>C NP_001035.1:p.Arg344=
NM_001044.5:c.1030A>C MANE Select NP_001035.1:p.Arg344=
Search 100 bp 5'
Search 100 bp 3'