Canonical Allele Identifier: CA404021563

Gene: CDKN2D

Linked Data

• gnomAD v4: 19-10568569-G-C
• MyVariant Identifiers: chr19:g.10679245G>C (hg19) ; chr19:g.10568569G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10568569G>C , CM000681.2:g.10568569G>C	GRCh38
NC_000019.9:g.10679245G>C , CM000681.1:g.10679245G>C	GRCh37
NC_000019.8:g.10540245G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000393599.3:c.85C>G MANE Select	ENSP00000377224.1:p.His29Asp
ENST00000335766.2:c.85C>G	ENSP00000337056.1:p.His29Asp
ENST00000393599.2:c.85C>G	ENSP00000377224.1:p.His29Asp
NM_001800.3:c.85C>G	NP_001791.1:p.His29Asp
NM_079421.2:c.85C>G	NP_524145.1:p.His29Asp
NM_001800.4:c.85C>G MANE Select	NP_001791.1:p.His29Asp
NM_079421.3:c.85C>G	NP_524145.1:p.His29Asp