Canonical Allele Identifier: CA660461789

Gene: SLC18A2

Linked Data

• dbSNP Id: rs1443240018
• MyVariant Identifiers: chr10:g.119022568C>T (hg19) ; chr10:g.117263057C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.117263057C>T , CM000672.2:g.117263057C>T	GRCh38
NC_000010.10:g.119022568C>T , CM000672.1:g.119022568C>T	GRCh37
NC_000010.9:g.119012558C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644641.2:c.992-3676C>T MANE Select	ENSP00000496339.1:n.992-3676C>T
ENST00000298472.9:c.992-3676C>T	ENSP00000298472.5:n.992-3676C>T
ENST00000497497.1:n.1408-3676C>T
NM_003054.4:c.992-3676C>T	NP_003045.2:n.992-3676C>T
NM_003054.5:c.992-3676C>T	NP_003045.2:n.992-3676C>T
NM_003054.6:c.992-3676C>T MANE Select	NP_003045.2:n.992-3676C>T