Canonical Allele Identifier: CA404021606
Gene: CDKN2D HGNC NCBI

Linked Data

gnomAD v4: 19-10568580-C-G
MyVariant Identifiers: chr19:g.10679256C>G (hg19) chr19:g.10568580C>G (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000393599.3:c.74G>C MANE Select ENSP00000377224.1:p.Arg25Pro
ENST00000335766.2:c.74G>C ENSP00000337056.1:p.Arg25Pro
ENST00000393599.2:c.74G>C ENSP00000377224.1:p.Arg25Pro
NM_001800.3:c.74G>C NP_001791.1:p.Arg25Pro
NM_079421.2:c.74G>C NP_524145.1:p.Arg25Pro
NM_001800.4:c.74G>C MANE Select NP_001791.1:p.Arg25Pro
NM_079421.3:c.74G>C NP_524145.1:p.Arg25Pro
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