Canonical Allele Identifier: CA1939105932
Gene: SLC18A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117262939T= , CM000672.2:g.117262939T= GRCh38
NC_000010.10:g.119022450T= , CM000672.1:g.119022450T= GRCh37
NC_000010.9:g.119012440T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000644641.2:c.992-3794T= MANE Select ENSP00000496339.1:n.992-3794T=
ENST00000298472.9:c.992-3794T= ENSP00000298472.5:n.992-3794T=
ENST00000497497.1:n.1408-3794T=
NM_003054.4:c.992-3794T= NP_003045.2:n.992-3794T=
NM_003054.5:c.992-3794T= NP_003045.2:n.992-3794T=
NM_003054.6:c.992-3794T= MANE Select NP_003045.2:n.992-3794T=