Canonical Allele Identifier: CA1939111274
Gene: SLC18A2 HGNC NCBI

Linked Data

dbSNP Id: rs1844459029

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117274207G>T , CM000672.2:g.117274207G>T GRCh38
NC_000010.10:g.119033718G>T , CM000672.1:g.119033718G>T GRCh37
NC_000010.9:g.119023708G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000644641.2:c.1441-2955G>T MANE Select ENSP00000496339.1:n.1441-2955G>T
ENST00000298472.9:c.1441-2955G>T ENSP00000298472.5:n.1441-2955G>T
ENST00000497497.1:n.1857-2955G>T
NM_003054.4:c.1441-2955G>T NP_003045.2:n.1441-2955G>T
NM_003054.5:c.1441-2955G>T NP_003045.2:n.1441-2955G>T
NM_003054.6:c.1441-2955G>T MANE Select NP_003045.2:n.1441-2955G>T