Canonical Allele Identifier: CA112961444
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1019795632
gnomAD v3: 5-1410936-A-G
gnomAD v4: 5-1410936-A-G
MyVariant Identifiers: chr5:g.1411051A>G (hg19) chr5:g.1410936A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1410936A>G , CM000667.2:g.1410936A>G GRCh38
NC_000005.9:g.1411051A>G , CM000667.1:g.1411051A>G GRCh37
NC_000005.8:g.1464051A>G NCBI36
NG_015885.1:g.39493T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1269+307T>C MANE Select ENSP00000270349.9:n.1269+307T>C
ENST00000270349.11:c.1269+307T>C ENSP00000270349.9:n.1269+307T>C
NM_001044.4:c.1269+307T>C NP_001035.1:n.1269+307T>C
NM_001044.5:c.1269+307T>C MANE Select NP_001035.1:n.1269+307T>C
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