Canonical Allele Identifier: CA6457352
Gene: CDKN1B HGNC NCBI

Linked Data

dbSNP Id: rs202167434
ExAC: 12:12870765 G / C
gnomAD v2: 12-12870765-G-C
gnomAD v4: 12-12717831-G-C
MyVariant Identifiers: chr12:g.12870765G>C (hg19) chr12:g.12717831G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12717831G>C , CM000674.2:g.12717831G>C GRCh38
NC_000012.11:g.12870765G>C , CM000674.1:g.12870765G>C GRCh37
NC_000012.10:g.12762032G>C NCBI36
NG_016341.1:g.5464G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.-9G>C ENSP00000507272.1:n.-9G>C
ENST00000682620.1:n.1631-994G>C
ENST00000684771.1:n.585-994G>C
ENST00000228872.9:c.-9G>C MANE Select ENSP00000228872.4:n.-9G>C
ENST00000228872.8:c.-9G>C ENSP00000228872.4:n.-9G>C
ENST00000396340.1:c.-9G>C ENSP00000379629.1:n.-9G>C
ENST00000477087.1:n.155-994G>C
NM_004064.4:c.-9G>C NP_004055.1:n.-9G>C
NM_004064.5:c.-9G>C MANE Select NP_004055.1:n.-9G>C
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