Canonical Allele Identifier: CA112954538
Gene: SLC6A3 HGNC NCBI

Linked Data

dbSNP Id: rs891109645
gnomAD v3: 5-1395025-A-C
gnomAD v4: 5-1395025-A-C
MyVariant Identifiers: chr5:g.1395025A>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1395025A>C , CM000667.2:g.1395025A>C GRCh38
NC_000005.9:g.1395140A>C , CM000667.1:g.1395140A>C GRCh37
NC_000005.8:g.1448140A>C NCBI36
NG_015885.1:g.55404T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000270349.12:c.1840-267T>G MANE Select ENSP00000270349.9:n.1840-267T>G
ENST00000270349.11:c.1840-267T>G ENSP00000270349.9:n.1840-267T>G
ENST00000512002.2:n.221-267T>G
NM_001044.4:c.1840-267T>G NP_001035.1:n.1840-267T>G
NM_001044.5:c.1840-267T>G MANE Select NP_001035.1:n.1840-267T>G