Canonical Allele Identifier: CA2017047398
Gene: CDKN1B HGNC NCBI
GPR19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12717719G= , CM000674.2:g.12717719G= GRCh38
NC_000012.11:g.12870653G= , CM000674.1:g.12870653G= GRCh37
NC_000012.10:g.12761920G= NCBI36
NG_016341.1:g.5352G=

Transcript Alleles

HGVS Amino-acid change
ENST00000614874.2:c.-121G= (CDKN1B) ENSP00000507272.1:n.-121G=
ENST00000682620.1:n.1631-1106G= (CDKN1B)
ENST00000684771.1:n.585-1106G= (CDKN1B)
ENST00000228872.9:c.-121G= (CDKN1B) MANE Select ENSP00000228872.4:n.-121G=
ENST00000228872.8:c.-121G= (CDKN1B) ENSP00000228872.4:n.-121G=
ENST00000477087.1:n.155-1106G= (CDKN1B)
NM_004064.4:c.-121G= (CDKN1B) NP_004055.1:n.-121G=
XM_011520623.3:c.-2213C= (GPR19) XP_011518925.1:n.-2213C=
XM_017019216.2:c.-2241C= (GPR19) XP_016874705.1:n.-2241C=
NM_004064.5:c.-121G= (CDKN1B) MANE Select NP_004055.1:n.-121G=