Canonical Allele Identifier: CA112963248

Gene: SLC6A3

Linked Data

• dbSNP Id: rs113697108
• MyVariant Identifiers: chr5:g.1414775A>G (hg19) ; chr5:g.1414660A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1414660A>G , CM000667.2:g.1414660A>G	GRCh38
NC_000005.9:g.1414775A>G , CM000667.1:g.1414775A>G	GRCh37
NC_000005.8:g.1467775A>G	NCBI36
NG_015885.1:g.35769T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270349.12:c.1156+31T>C MANE Select	ENSP00000270349.9:n.1156+31T>C
ENST00000270349.11:c.1156+31T>C	ENSP00000270349.9:n.1156+31T>C
NM_001044.4:c.1156+31T>C	NP_001035.1:n.1156+31T>C
NM_001044.5:c.1156+31T>C MANE Select	NP_001035.1:n.1156+31T>C