Canonical Allele Identifier: CA112961517

Gene: SLC6A3

Linked Data

• dbSNP Id: rs981961765
• MyVariant Identifiers: chr5:g.1411168C>G (hg19) ; chr5:g.1411053C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1411053C>G , CM000667.2:g.1411053C>G	GRCh38
NC_000005.9:g.1411168C>G , CM000667.1:g.1411168C>G	GRCh37
NC_000005.8:g.1464168C>G	NCBI36
NG_015885.1:g.39376G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270349.12:c.1269+190G>C MANE Select	ENSP00000270349.9:n.1269+190G>C
ENST00000270349.11:c.1269+190G>C	ENSP00000270349.9:n.1269+190G>C
NM_001044.4:c.1269+190G>C	NP_001035.1:n.1269+190G>C
NM_001044.5:c.1269+190G>C MANE Select	NP_001035.1:n.1269+190G>C