Canonical Allele Identifier: CA404021608
Gene: CDKN2D HGNC NCBI

Linked Data

dbSNP Id: rs1232079509
gnomAD v2: 19-10679256-C-T
gnomAD v4: 19-10568580-C-T
MyVariant Identifiers: chr19:g.10679256C>T (hg19) chr19:g.10568580C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10568580C>T , CM000681.2:g.10568580C>T GRCh38
NC_000019.9:g.10679256C>T , CM000681.1:g.10679256C>T GRCh37
NC_000019.8:g.10540256C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000393599.3:c.74G>A MANE Select ENSP00000377224.1:p.Arg25His
ENST00000335766.2:c.74G>A ENSP00000337056.1:p.Arg25His
ENST00000393599.2:c.74G>A ENSP00000377224.1:p.Arg25His
NM_001800.3:c.74G>A NP_001791.1:p.Arg25His
NM_079421.2:c.74G>A NP_524145.1:p.Arg25His
NM_001800.4:c.74G>A MANE Select NP_001791.1:p.Arg25His
NM_079421.3:c.74G>A NP_524145.1:p.Arg25His
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