Canonical Allele Identifier: CA214689767
Gene: SLC18A2 HGNC NCBI

Linked Data

dbSNP Id: rs141747487
gnomAD v2: 10-119022658-C-T
gnomAD v3: 10-117263147-C-T
gnomAD v4: 10-117263147-C-T
MyVariant Identifiers: chr10:g.119022658C>T (hg19) chr10:g.117263147C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117263147C>T , CM000672.2:g.117263147C>T GRCh38
NC_000010.10:g.119022658C>T , CM000672.1:g.119022658C>T GRCh37
NC_000010.9:g.119012648C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000644641.2:c.992-3586C>T MANE Select ENSP00000496339.1:n.992-3586C>T
ENST00000298472.9:c.992-3586C>T ENSP00000298472.5:n.992-3586C>T
ENST00000497497.1:n.1408-3586C>T
NM_003054.4:c.992-3586C>T NP_003045.2:n.992-3586C>T
NM_003054.5:c.992-3586C>T NP_003045.2:n.992-3586C>T
NM_003054.6:c.992-3586C>T MANE Select NP_003045.2:n.992-3586C>T
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