Canonical Allele Identifier: CA2789645163
Gene: SLC18A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117263057C>A , CM000672.2:g.117263057C>A GRCh38
NC_000010.10:g.119022568C>A , CM000672.1:g.119022568C>A GRCh37
NC_000010.9:g.119012558C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000644641.2:c.992-3676C>A MANE Select ENSP00000496339.1:n.992-3676C>A
ENST00000298472.9:c.992-3676C>A ENSP00000298472.5:n.992-3676C>A
ENST00000497497.1:n.1408-3676C>A
NM_003054.4:c.992-3676C>A NP_003045.2:n.992-3676C>A
NM_003054.5:c.992-3676C>A NP_003045.2:n.992-3676C>A
NM_003054.6:c.992-3676C>A MANE Select NP_003045.2:n.992-3676C>A
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