Canonical Allele Identifier: CA2017047337
Gene: CDKN1B HGNC NCBI
GPR19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12717656T= , CM000674.2:g.12717656T= GRCh38
NC_000012.11:g.12870590T= , CM000674.1:g.12870590T= GRCh37
NC_000012.10:g.12761857T= NCBI36
NG_016341.1:g.5289T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.-184T= (CDKN1B) ENSP00000507272.1:n.-184T=
ENST00000682620.1:n.1631-1169T= (CDKN1B)
ENST00000684771.1:n.585-1169T= (CDKN1B)
ENST00000228872.9:c.-184T= (CDKN1B) MANE Select ENSP00000228872.4:n.-184T=
ENST00000228872.8:c.-184T= (CDKN1B) ENSP00000228872.4:n.-184T=
ENST00000477087.1:n.155-1169T= (CDKN1B)
NM_004064.4:c.-184T= (CDKN1B) NP_004055.1:n.-184T=
XM_011520623.3:c.-2150A= (GPR19) XP_011518925.1:n.-2150A=
XM_017019216.2:c.-2178A= (GPR19) XP_016874705.1:n.-2178A=
NM_004064.5:c.-184T= (CDKN1B) MANE Select NP_004055.1:n.-184T=
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