Canonical Allele Identifier: CA1939111284

Gene: SLC18A2

Linked Data

• dbSNP Id: rs1844459299

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.117274221del , CM000672.2:g.117274221del	GRCh38
NC_000010.10:g.119033732del , CM000672.1:g.119033732del	GRCh37
NC_000010.9:g.119023722del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000644641.2:c.1441-2941del MANE Select	ENSP00000496339.1:n.1441-2941del
ENST00000298472.9:c.1441-2941del	ENSP00000298472.5:n.1441-2941del
ENST00000497497.1:n.1857-2941del
NM_003054.4:c.1441-2941del	NP_003045.2:n.1441-2941del
NM_003054.5:c.1441-2941del	NP_003045.2:n.1441-2941del
NM_003054.6:c.1441-2941del MANE Select	NP_003045.2:n.1441-2941del