Canonical Allele Identifier: CA1939106009
Gene: SLC18A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117263132A= , CM000672.2:g.117263132A= GRCh38
NC_000010.10:g.119022643A= , CM000672.1:g.119022643A= GRCh37
NC_000010.9:g.119012633A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000644641.2:c.992-3601A= MANE Select ENSP00000496339.1:n.992-3601A=
ENST00000298472.9:c.992-3601A= ENSP00000298472.5:n.992-3601A=
ENST00000497497.1:n.1408-3601A=
NM_003054.4:c.992-3601A= NP_003045.2:n.992-3601A=
NM_003054.5:c.992-3601A= NP_003045.2:n.992-3601A=
NM_003054.6:c.992-3601A= MANE Select NP_003045.2:n.992-3601A=
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