Canonical Allele Identifier: CA804997463

Gene: SLC6A3

Linked Data

• dbSNP Id: rs1165366856
• gnomAD v3: 5-1443568-G-C
• gnomAD v4: 5-1443568-G-C
• MyVariant Identifiers: chr5:g.1443683G>C (hg19) ; chr5:g.1443568G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1443568G>C , CM000667.2:g.1443568G>C	GRCh38
NC_000005.9:g.1443683G>C , CM000667.1:g.1443683G>C	GRCh37
NC_000005.8:g.1496683G>C	NCBI36
NG_015885.1:g.6861C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270349.12:c.-45-326C>G MANE Select	ENSP00000270349.9:n.-45-326C>G
ENST00000270349.11:c.-45-326C>G	ENSP00000270349.9:n.-45-326C>G
NM_001044.4:c.-45-326C>G	NP_001035.1:n.-45-326C>G
NM_001044.5:c.-45-326C>G MANE Select	NP_001035.1:n.-45-326C>G