Canonical Allele Identifier: CA1939111287
Gene: SLC18A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117274224C= , CM000672.2:g.117274224C= GRCh38
NC_000010.10:g.119033735C= , CM000672.1:g.119033735C= GRCh37
NC_000010.9:g.119023725C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000644641.2:c.1441-2938C= MANE Select ENSP00000496339.1:n.1441-2938C=
ENST00000298472.9:c.1441-2938C= ENSP00000298472.5:n.1441-2938C=
ENST00000497497.1:n.1857-2938C=
NM_003054.4:c.1441-2938C= NP_003045.2:n.1441-2938C=
NM_003054.5:c.1441-2938C= NP_003045.2:n.1441-2938C=
NM_003054.6:c.1441-2938C= MANE Select NP_003045.2:n.1441-2938C=