Canonical Allele Identifier: CA112968546

Gene: SLC6A3

Linked Data

• dbSNP Id: rs368576511
• MyVariant Identifiers: chr5:g.1423819C>G (hg19) ; chr5:g.1423704C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1423704C>G , CM000667.2:g.1423704C>G	GRCh38
NC_000005.9:g.1423819C>G , CM000667.1:g.1423819C>G	GRCh37
NC_000005.8:g.1476819C>G	NCBI36
NG_015885.1:g.26725G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000270349.12:c.654-1690G>C MANE Select	ENSP00000270349.9:n.654-1690G>C
ENST00000270349.11:c.654-1690G>C	ENSP00000270349.9:n.654-1690G>C
NM_001044.4:c.654-1690G>C	NP_001035.1:n.654-1690G>C
NM_001044.5:c.654-1690G>C MANE Select	NP_001035.1:n.654-1690G>C