Canonical Allele Identifier: CA2017047136
Gene: CDKN1B HGNC NCBI
GPR19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12717422T= , CM000674.2:g.12717422T= GRCh38
NC_000012.11:g.12870356T= , CM000674.1:g.12870356T= GRCh37
NC_000012.10:g.12761623T= NCBI36
NG_016341.1:g.5055T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.-418T= (CDKN1B) ENSP00000507272.1:n.-418T=
ENST00000682620.1:n.1631-1403T= (CDKN1B)
ENST00000684771.1:n.585-1403T= (CDKN1B)
ENST00000228872.9:c.-418T= (CDKN1B) MANE Select ENSP00000228872.4:n.-418T=
ENST00000228872.8:c.-418T= (CDKN1B) ENSP00000228872.4:n.-418T=
ENST00000477087.1:n.155-1403T= (CDKN1B)
NM_004064.4:c.-418T= (CDKN1B) NP_004055.1:n.-418T=
XM_011520623.3:c.-1916A= (GPR19) XP_011518925.1:n.-1916A=
XM_017019216.2:c.-1944A= (GPR19) XP_016874705.1:n.-1944A=
NM_004064.5:c.-418T= (CDKN1B) MANE Select NP_004055.1:n.-418T=
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