Canonical Allele Identifier: CA404021547
Gene: CDKN2D HGNC NCBI

Linked Data

dbSNP Id: rs1402557674

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10568565C>T , CM000681.2:g.10568565C>T GRCh38
NC_000019.9:g.10679241C>T , CM000681.1:g.10679241C>T GRCh37
NC_000019.8:g.10540241C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393599.3:c.89G>A MANE Select ENSP00000377224.1:p.Arg30Gln
ENST00000335766.2:c.89G>A ENSP00000337056.1:p.Arg30Gln
ENST00000393599.2:c.89G>A ENSP00000377224.1:p.Arg30Gln
NM_001800.3:c.89G>A NP_001791.1:p.Arg30His
NM_079421.2:c.89G>A NP_524145.1:p.Arg30His
NM_001800.4:c.89G>A MANE Select NP_001791.1:p.Arg30Gln
NM_079421.3:c.89G>A NP_524145.1:p.Arg30Gln