Canonical Allele Identifier: CA783185503
Gene: CDKN2D HGNC NCBI

Linked Data

dbSNP Id: rs1265556131
gnomAD v3: 19-10568391-G-C
gnomAD v4: 19-10568391-G-C
MyVariant Identifiers: chr19:g.10679067G>C (hg19) chr19:g.10568391G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10568391G>C , CM000681.2:g.10568391G>C GRCh38
NC_000019.9:g.10679067G>C , CM000681.1:g.10679067G>C GRCh37
NC_000019.8:g.10540067G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393599.3:c.141+122C>G MANE Select ENSP00000377224.1:n.141+122C>G
ENST00000335766.2:c.141+122C>G ENSP00000337056.1:n.141+122C>G
ENST00000393599.2:c.141+122C>G ENSP00000377224.1:n.141+122C>G
NM_001800.3:c.141+122C>G NP_001791.1:n.141+122C>G
NM_079421.2:c.141+122C>G NP_524145.1:n.141+122C>G
NM_001800.4:c.141+122C>G MANE Select NP_001791.1:n.141+122C>G
NM_079421.3:c.141+122C>G NP_524145.1:n.141+122C>G
Search 100 bp 5'
Search 100 bp 3'