Canonical Allele Identifier: CA1939105925
Gene: SLC18A2 HGNC NCBI

Linked Data

dbSNP Id: rs1844310338
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117262922G>A , CM000672.2:g.117262922G>A GRCh38
NC_000010.10:g.119022433G>A , CM000672.1:g.119022433G>A GRCh37
NC_000010.9:g.119012423G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000644641.2:c.992-3811G>A MANE Select ENSP00000496339.1:n.992-3811G>A
ENST00000298472.9:c.992-3811G>A ENSP00000298472.5:n.992-3811G>A
ENST00000497497.1:n.1408-3811G>A
NM_003054.4:c.992-3811G>A NP_003045.2:n.992-3811G>A
NM_003054.5:c.992-3811G>A NP_003045.2:n.992-3811G>A
NM_003054.6:c.992-3811G>A MANE Select NP_003045.2:n.992-3811G>A
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