Canonical Allele Identifier: CA1939105908
Gene: SLC18A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117262887C= , CM000672.2:g.117262887C= GRCh38
NC_000010.10:g.119022398C= , CM000672.1:g.119022398C= GRCh37
NC_000010.9:g.119012388C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000644641.2:c.992-3846C= MANE Select ENSP00000496339.1:n.992-3846C=
ENST00000298472.9:c.992-3846C= ENSP00000298472.5:n.992-3846C=
ENST00000497497.1:n.1408-3846C=
NM_003054.4:c.992-3846C= NP_003045.2:n.992-3846C=
NM_003054.5:c.992-3846C= NP_003045.2:n.992-3846C=
NM_003054.6:c.992-3846C= MANE Select NP_003045.2:n.992-3846C=
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