Canonical Allele Identifier: CA804997716
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs1254618607
gnomAD v3: 5-1444213-T-C
gnomAD v4: 5-1444213-T-C
MyVariant Identifiers: chr5:g.1444328T>C (hg19) chr5:g.1444213T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1444213T>C , CM000667.2:g.1444213T>C GRCh38
NC_000005.9:g.1444328T>C , CM000667.1:g.1444328T>C GRCh37
NC_000005.8:g.1497328T>C NCBI36
NG_015885.1:g.6216A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000270349.12:c.-45-971A>G MANE Select ENSP00000270349.9:n.-45-971A>G
ENST00000270349.11:c.-45-971A>G ENSP00000270349.9:n.-45-971A>G
NM_001044.4:c.-45-971A>G NP_001035.1:n.-45-971A>G
NM_001044.5:c.-45-971A>G MANE Select NP_001035.1:n.-45-971A>G
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