Canonical Allele Identifier: CA1939106066

Gene: SLC18A2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.117263237C= , CM000672.2:g.117263237C=	GRCh38
NC_000010.10:g.119022748C= , CM000672.1:g.119022748C=	GRCh37
NC_000010.9:g.119012738C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644641.2:c.992-3496C= MANE Select	ENSP00000496339.1:n.992-3496C=
ENST00000298472.9:c.992-3496C=	ENSP00000298472.5:n.992-3496C=
ENST00000497497.1:n.1408-3496C=
NM_003054.4:c.992-3496C=	NP_003045.2:n.992-3496C=
NM_003054.5:c.992-3496C=	NP_003045.2:n.992-3496C=
NM_003054.6:c.992-3496C= MANE Select	NP_003045.2:n.992-3496C=