Canonical Allele Identifier: CA214695491
Gene: SLC18A2 HGNC NCBI

Linked Data

dbSNP Id: rs1033172849
gnomAD v3: 10-117274327-G-T
gnomAD v4: 10-117274327-G-T
MyVariant Identifiers: chr10:g.119033838G>T (hg19) chr10:g.117274327G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.117274327G>T , CM000672.2:g.117274327G>T GRCh38
NC_000010.10:g.119033838G>T , CM000672.1:g.119033838G>T GRCh37
NC_000010.9:g.119023828G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000644641.2:c.1441-2835G>T MANE Select ENSP00000496339.1:n.1441-2835G>T
ENST00000298472.9:c.1441-2835G>T ENSP00000298472.5:n.1441-2835G>T
ENST00000497497.1:n.1857-2835G>T
NM_003054.4:c.1441-2835G>T NP_003045.2:n.1441-2835G>T
NM_003054.5:c.1441-2835G>T NP_003045.2:n.1441-2835G>T
NM_003054.6:c.1441-2835G>T MANE Select NP_003045.2:n.1441-2835G>T
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