Canonical Allele Identifier: CA112970449
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs894851208
gnomAD v2: 5-1443861-A-G
gnomAD v3: 5-1443746-A-G
gnomAD v4: 5-1443746-A-G
MyVariant Identifiers: chr5:g.1443861A>G (hg19) chr5:g.1443746A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1443746A>G , CM000667.2:g.1443746A>G GRCh38
NC_000005.9:g.1443861A>G , CM000667.1:g.1443861A>G GRCh37
NC_000005.8:g.1496861A>G NCBI36
NG_015885.1:g.6683T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.-45-504T>C MANE Select ENSP00000270349.9:n.-45-504T>C
ENST00000270349.11:c.-45-504T>C ENSP00000270349.9:n.-45-504T>C
NM_001044.4:c.-45-504T>C NP_001035.1:n.-45-504T>C
NM_001044.5:c.-45-504T>C MANE Select NP_001035.1:n.-45-504T>C
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