Canonical Allele Identifier: CA112958617

Gene: SLC6A3

Linked Data

• dbSNP Id: rs1038498209
• MyVariant Identifiers: chr5:g.1428292C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1428292C>G , CM000667.2:g.1428292C>G	GRCh38
NC_000005.9:g.1428407C>G , CM000667.1:g.1428407C>G	GRCh37
NC_000005.8:g.1481407C>G	NCBI36
NG_015885.1:g.22137G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270349.12:c.653+4172G>C MANE Select	ENSP00000270349.9:n.653+4172G>C
ENST00000270349.11:c.653+4172G>C	ENSP00000270349.9:n.653+4172G>C
NM_001044.4:c.653+4172G>C	NP_001035.1:n.653+4172G>C
NM_001044.5:c.653+4172G>C MANE Select	NP_001035.1:n.653+4172G>C