Canonical Allele Identifier: CA383968849

Gene: CDKN1B

Linked Data

• ClinVar Variation Id: 1524053
• ClinVar RCV Id: RCV002031432
• dbSNP Id: rs2136355606
• gnomAD v4: 12-12717969-G-T
• MyVariant Identifiers: chr12:g.12870903G>T (hg19) ; chr12:g.12717969G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12717969G>T , CM000674.2:g.12717969G>T	GRCh38
NC_000012.11:g.12870903G>T , CM000674.1:g.12870903G>T	GRCh37
NC_000012.10:g.12762170G>T	NCBI36
NG_016341.1:g.5602G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614874.2:c.130G>T	ENSP00000507272.1:p.Asp44Tyr
ENST00000682620.1:n.1631-856G>T
ENST00000684771.1:n.585-856G>T
ENST00000228872.9:c.130G>T MANE Select	ENSP00000228872.4:p.Asp44Tyr
ENST00000228872.8:c.130G>T	ENSP00000228872.4:p.Asp44Tyr
ENST00000396340.1:c.130G>T	ENSP00000379629.1:p.Asp44Tyr
ENST00000442489.1:c.109G>T	ENSP00000407597.1:p.Asp37Tyr
ENST00000477087.1:n.155-856G>T
NM_004064.4:c.130G>T	NP_004055.1:p.Asp44Tyr
NM_004064.5:c.130G>T MANE Select	NP_004055.1:p.Asp44Tyr