Canonical Allele Identifier: CA9197600
Gene: CDKN2D HGNC NCBI

Linked Data

dbSNP Id: rs552186811
ExAC: 19:10679253 C / A
gnomAD v2: 19-10679253-C-A
gnomAD v3: 19-10568577-C-A
gnomAD v4: 19-10568577-C-A
MyVariant Identifiers: chr19:g.10679253C>A (hg19) chr19:g.10568577C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10568577C>A , CM000681.2:g.10568577C>A GRCh38
NC_000019.9:g.10679253C>A , CM000681.1:g.10679253C>A GRCh37
NC_000019.8:g.10540253C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393599.3:c.77G>T MANE Select ENSP00000377224.1:p.Arg26Leu
ENST00000335766.2:c.77G>T ENSP00000337056.1:p.Arg26Leu
ENST00000393599.2:c.77G>T ENSP00000377224.1:p.Arg26Leu
NM_001800.3:c.77G>T NP_001791.1:p.Arg26Leu
NM_079421.2:c.77G>T NP_524145.1:p.Arg26Leu
NM_001800.4:c.77G>T MANE Select NP_001791.1:p.Arg26Leu
NM_079421.3:c.77G>T NP_524145.1:p.Arg26Leu
Search 100 bp 5'
Search 100 bp 3'