Canonical Allele Identifier: CA684983086
Gene: CDKN1B HGNC NCBI

Linked Data

dbSNP Id: rs1397433569
gnomAD v3: 12-12720373-TTTC-T
gnomAD v4: 12-12720373-TTTC-T
MyVariant Identifiers: chr12:g.12873308_12873310del (hg19) chr12:g.12720374_12720376del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12720375_12720377del , CM000674.2:g.12720375_12720377del GRCh38
NC_000012.11:g.12873309_12873311del , CM000674.1:g.12873309_12873311del GRCh37
NC_000012.10:g.12764576_12764578del NCBI36
NG_016341.1:g.8008_8010del

Transcript Alleles

HGVS Amino-acid change
ENST00000614874.2:c.*1429_*1431del ENSP00000507272.1:n.*1429_*1431del
ENST00000682620.1:n.1761-661_1761-659del
ENST00000684771.1:n.715-661_715-659del
ENST00000228872.9:c.*9-661_*9-659del MANE Select ENSP00000228872.4:n.*9-661_*9-659del
ENST00000228872.8:c.*9-661_*9-659del ENSP00000228872.4:n.*9-661_*9-659del
ENST00000396340.1:c.476-690_476-688del ENSP00000379629.1:n.476-690_476-688del
ENST00000442489.1:c.324-661_324-659del ENSP00000407597.1:n.324-661_324-659del
ENST00000477087.1:n.285-661_285-659del
NM_004064.4:c.*9-661_*9-659del NP_004055.1:n.*9-661_*9-659del
NM_004064.5:c.*9-661_*9-659del MANE Select NP_004055.1:n.*9-661_*9-659del
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