Canonical Allele Identifier: CA1939105918
Gene: SLC18A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117262905C= , CM000672.2:g.117262905C= GRCh38
NC_000010.10:g.119022416C= , CM000672.1:g.119022416C= GRCh37
NC_000010.9:g.119012406C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000644641.2:c.992-3828C= MANE Select ENSP00000496339.1:n.992-3828C=
ENST00000298472.9:c.992-3828C= ENSP00000298472.5:n.992-3828C=
ENST00000497497.1:n.1408-3828C=
NM_003054.4:c.992-3828C= NP_003045.2:n.992-3828C=
NM_003054.5:c.992-3828C= NP_003045.2:n.992-3828C=
NM_003054.6:c.992-3828C= MANE Select NP_003045.2:n.992-3828C=