Canonical Allele Identifier: CA233059507
Gene: CDKN1B HGNC NCBI

Linked Data

dbSNP Id: rs998060990
MyVariant Identifiers: chr12:g.12870772A>G (hg19) chr12:g.12717838A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12717838A>G , CM000674.2:g.12717838A>G GRCh38
NC_000012.11:g.12870772A>G , CM000674.1:g.12870772A>G GRCh37
NC_000012.10:g.12762039A>G NCBI36
NG_016341.1:g.5471A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000614874.2:c.-2A>G ENSP00000507272.1:n.-2A>G
ENST00000682620.1:n.1631-987A>G
ENST00000684771.1:n.585-987A>G
ENST00000228872.9:c.-2A>G MANE Select ENSP00000228872.4:n.-2A>G
ENST00000228872.8:c.-2A>G ENSP00000228872.4:n.-2A>G
ENST00000396340.1:c.-2A>G ENSP00000379629.1:n.-2A>G
ENST00000477087.1:n.155-987A>G
NM_004064.4:c.-2A>G NP_004055.1:n.-2A>G
NM_004064.5:c.-2A>G MANE Select NP_004055.1:n.-2A>G
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