Canonical Allele Identifier: CA505394444
Gene: CDKN2D HGNC NCBI

Linked Data

dbSNP Id: rs1916967625
MyVariant Identifiers: chr19:g.10679255G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10568579G>A , CM000681.2:g.10568579G>A GRCh38
NC_000019.9:g.10679255G>A , CM000681.1:g.10679255G>A GRCh37
NC_000019.8:g.10540255G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000393599.3:c.75C>T MANE Select ENSP00000377224.1:p.Arg25=
ENST00000335766.2:c.75C>T ENSP00000337056.1:p.Arg25=
ENST00000393599.2:c.75C>T ENSP00000377224.1:p.Arg25=
NM_001800.3:c.75C>T NP_001791.1:p.Arg25=
NM_079421.2:c.75C>T NP_524145.1:p.Arg25=
NM_001800.4:c.75C>T MANE Select NP_001791.1:p.Arg25=
NM_079421.3:c.75C>T NP_524145.1:p.Arg25=