Canonical Allele Identifier: CA6457396
Gene: CDKN1B HGNC NCBI

Linked Data

ClinVar Variation Id: 662565
ClinVar RCV Id: RCV000820230 RCV001012076
dbSNP Id: rs760647541
ExAC: 12:12870927 A / T
gnomAD v2: 12-12870927-A-T
gnomAD v3: 12-12717993-A-T
gnomAD v4: 12-12717993-A-T
MyVariant Identifiers: chr12:g.12870927A>T (hg19) chr12:g.12717993A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12717993A>T , CM000674.2:g.12717993A>T GRCh38
NC_000012.11:g.12870927A>T , CM000674.1:g.12870927A>T GRCh37
NC_000012.10:g.12762194A>T NCBI36
NG_016341.1:g.5626A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000614874.2:c.154A>T ENSP00000507272.1:p.Met52Leu
ENST00000682620.1:n.1631-832A>T
ENST00000684771.1:n.585-832A>T
ENST00000228872.9:c.154A>T MANE Select ENSP00000228872.4:p.Met52Leu
ENST00000228872.8:c.154A>T ENSP00000228872.4:p.Met52Leu
ENST00000396340.1:c.154A>T ENSP00000379629.1:p.Met52Leu
ENST00000442489.1:c.133A>T ENSP00000407597.1:p.Met45Leu
ENST00000477087.1:n.155-832A>T
NM_004064.4:c.154A>T NP_004055.1:p.Met52Leu
NM_004064.5:c.154A>T MANE Select NP_004055.1:p.Met52Leu
Search 100 bp 5'
Search 100 bp 3'