Canonical Allele Identifier: CA1939111292
Gene: SLC18A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117274248T= , CM000672.2:g.117274248T= GRCh38
NC_000010.10:g.119033759T= , CM000672.1:g.119033759T= GRCh37
NC_000010.9:g.119023749T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000644641.2:c.1441-2914T= MANE Select ENSP00000496339.1:n.1441-2914T=
ENST00000298472.9:c.1441-2914T= ENSP00000298472.5:n.1441-2914T=
ENST00000497497.1:n.1857-2914T=
NM_003054.4:c.1441-2914T= NP_003045.2:n.1441-2914T=
NM_003054.5:c.1441-2914T= NP_003045.2:n.1441-2914T=
NM_003054.6:c.1441-2914T= MANE Select NP_003045.2:n.1441-2914T=
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