Canonical Allele Identifier: CA653823591
Gene: SLC18A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117262910T>A , CM000672.2:g.117262910T>A GRCh38
NC_000010.10:g.119022421T>A , CM000672.1:g.119022421T>A GRCh37
NC_000010.9:g.119012411T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000644641.2:c.992-3823T>A MANE Select ENSP00000496339.1:n.992-3823T>A
ENST00000298472.9:c.992-3823T>A ENSP00000298472.5:n.992-3823T>A
ENST00000497497.1:n.1408-3823T>A
NM_003054.4:c.992-3823T>A NP_003045.2:n.992-3823T>A
NM_003054.5:c.992-3823T>A NP_003045.2:n.992-3823T>A
NM_003054.6:c.992-3823T>A MANE Select NP_003045.2:n.992-3823T>A