Canonical Allele Identifier: CA383969376
Gene: CDKN1B HGNC NCBI

Linked Data

gnomAD v4: 12-12718030-T-G
MyVariant Identifiers: chr12:g.12870964T>G (hg19) chr12:g.12718030T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12718030T>G , CM000674.2:g.12718030T>G GRCh38
NC_000012.11:g.12870964T>G , CM000674.1:g.12870964T>G GRCh37
NC_000012.10:g.12762231T>G NCBI36
NG_016341.1:g.5663T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000614874.2:c.191T>G ENSP00000507272.1:p.Phe64Cys
ENST00000682620.1:n.1631-795T>G
ENST00000684771.1:n.585-795T>G
ENST00000228872.9:c.191T>G MANE Select ENSP00000228872.4:p.Phe64Cys
ENST00000228872.8:c.191T>G ENSP00000228872.4:p.Phe64Cys
ENST00000396340.1:c.191T>G ENSP00000379629.1:p.Phe64Cys
ENST00000442489.1:c.170T>G ENSP00000407597.1:p.Phe57Cys
ENST00000477087.1:n.155-795T>G
NM_004064.4:c.191T>G NP_004055.1:p.Phe64Cys
NM_004064.5:c.191T>G MANE Select NP_004055.1:p.Phe64Cys
Search 100 bp 5'
Search 100 bp 3'