Canonical Allele Identifier: CA383968143

Gene: CDKN1B

Linked Data

• dbSNP Id: rs1411029555
• gnomAD v2: 12-12870820-T-G
• gnomAD v4: 12-12717886-T-G
• MyVariant Identifiers: chr12:g.12870820T>G (hg19) ; chr12:g.12717886T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12717886T>G , CM000674.2:g.12717886T>G	GRCh38
NC_000012.11:g.12870820T>G , CM000674.1:g.12870820T>G	GRCh37
NC_000012.10:g.12762087T>G	NCBI36
NG_016341.1:g.5519T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614874.2:c.47T>G	ENSP00000507272.1:p.Met16Arg
ENST00000682620.1:n.1631-939T>G
ENST00000684771.1:n.585-939T>G
ENST00000228872.9:c.47T>G MANE Select	ENSP00000228872.4:p.Met16Arg
ENST00000228872.8:c.47T>G	ENSP00000228872.4:p.Met16Arg
ENST00000396340.1:c.47T>G	ENSP00000379629.1:p.Met16Arg
ENST00000442489.1:c.26T>G	ENSP00000407597.1:p.Met9Arg
ENST00000477087.1:n.155-939T>G
NM_004064.4:c.47T>G	NP_004055.1:p.Met16Arg
NM_004064.5:c.47T>G MANE Select	NP_004055.1:p.Met16Arg