Canonical Allele Identifier: CA214689741
Gene: SLC18A2 HGNC NCBI

Linked Data

dbSNP Id: rs985955957
gnomAD v3: 10-117263116-A-G
gnomAD v4: 10-117263116-A-G
MyVariant Identifiers: chr10:g.119022627A>G (hg19) chr10:g.117263116A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117263116A>G , CM000672.2:g.117263116A>G GRCh38
NC_000010.10:g.119022627A>G , CM000672.1:g.119022627A>G GRCh37
NC_000010.9:g.119012617A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000644641.2:c.992-3617A>G MANE Select ENSP00000496339.1:n.992-3617A>G
ENST00000298472.9:c.992-3617A>G ENSP00000298472.5:n.992-3617A>G
ENST00000497497.1:n.1408-3617A>G
NM_003054.4:c.992-3617A>G NP_003045.2:n.992-3617A>G
NM_003054.5:c.992-3617A>G NP_003045.2:n.992-3617A>G
NM_003054.6:c.992-3617A>G MANE Select NP_003045.2:n.992-3617A>G
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