Canonical Allele Identifier: CA1939106046
Gene: SLC18A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117263192C= , CM000672.2:g.117263192C= GRCh38
NC_000010.10:g.119022703C= , CM000672.1:g.119022703C= GRCh37
NC_000010.9:g.119012693C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000644641.2:c.992-3541C= MANE Select ENSP00000496339.1:n.992-3541C=
ENST00000298472.9:c.992-3541C= ENSP00000298472.5:n.992-3541C=
ENST00000497497.1:n.1408-3541C=
NM_003054.4:c.992-3541C= NP_003045.2:n.992-3541C=
NM_003054.5:c.992-3541C= NP_003045.2:n.992-3541C=
NM_003054.6:c.992-3541C= MANE Select NP_003045.2:n.992-3541C=