Canonical Allele Identifier: CA783185501
Gene: CDKN2D HGNC NCBI

Linked Data

dbSNP Id: rs1485018064
gnomAD v3: 19-10568380-A-G
gnomAD v4: 19-10568380-A-G
MyVariant Identifiers: chr19:g.10679056A>G (hg19) chr19:g.10568380A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10568380A>G , CM000681.2:g.10568380A>G GRCh38
NC_000019.9:g.10679056A>G , CM000681.1:g.10679056A>G GRCh37
NC_000019.8:g.10540056A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393599.3:c.141+133T>C MANE Select ENSP00000377224.1:n.141+133T>C
ENST00000335766.2:c.141+133T>C ENSP00000337056.1:n.141+133T>C
ENST00000393599.2:c.141+133T>C ENSP00000377224.1:n.141+133T>C
NM_001800.3:c.141+133T>C NP_001791.1:n.141+133T>C
NM_079421.2:c.141+133T>C NP_524145.1:n.141+133T>C
NM_001800.4:c.141+133T>C MANE Select NP_001791.1:n.141+133T>C
NM_079421.3:c.141+133T>C NP_524145.1:n.141+133T>C
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