Canonical Allele Identifier: CA404021552
Gene: CDKN2D HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10568567G>C , CM000681.2:g.10568567G>C GRCh38
NC_000019.9:g.10679243G>C , CM000681.1:g.10679243G>C GRCh37
NC_000019.8:g.10540243G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393599.3:c.87C>G MANE Select ENSP00000377224.1:p.His29Gln
ENST00000335766.2:c.87C>G ENSP00000337056.1:p.His29Gln
ENST00000393599.2:c.87C>G ENSP00000377224.1:p.His29Gln
NM_001800.3:c.87C>G NP_001791.1:p.His29Gln
NM_079421.2:c.87C>G NP_524145.1:p.His29Gln
NM_001800.4:c.87C>G MANE Select NP_001791.1:p.His29Gln
NM_079421.3:c.87C>G NP_524145.1:p.His29Gln