Canonical Allele Identifier: CA653823593
Gene: SLC18A2 HGNC NCBI

Linked Data

COSMIC: COSN21333440
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117262945C>G , CM000672.2:g.117262945C>G GRCh38
NC_000010.10:g.119022456C>G , CM000672.1:g.119022456C>G GRCh37
NC_000010.9:g.119012446C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000644641.2:c.992-3788C>G MANE Select ENSP00000496339.1:n.992-3788C>G
ENST00000298472.9:c.992-3788C>G ENSP00000298472.5:n.992-3788C>G
ENST00000497497.1:n.1408-3788C>G
NM_003054.4:c.992-3788C>G NP_003045.2:n.992-3788C>G
NM_003054.5:c.992-3788C>G NP_003045.2:n.992-3788C>G
NM_003054.6:c.992-3788C>G MANE Select NP_003045.2:n.992-3788C>G
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