Canonical Allele Identifier: CA1939105913
Gene: SLC18A2 HGNC NCBI

Linked Data

dbSNP Id: rs1217380783

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117262893A>G , CM000672.2:g.117262893A>G GRCh38
NC_000010.10:g.119022404A>G , CM000672.1:g.119022404A>G GRCh37
NC_000010.9:g.119012394A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000644641.2:c.992-3840A>G MANE Select ENSP00000496339.1:n.992-3840A>G
ENST00000298472.9:c.992-3840A>G ENSP00000298472.5:n.992-3840A>G
ENST00000497497.1:n.1408-3840A>G
NM_003054.4:c.992-3840A>G NP_003045.2:n.992-3840A>G
NM_003054.5:c.992-3840A>G NP_003045.2:n.992-3840A>G
NM_003054.6:c.992-3840A>G MANE Select NP_003045.2:n.992-3840A>G