Canonical Allele Identifier: CA2617685023
Gene: CDKN1B HGNC NCBI
GPR19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12717406A>C , CM000674.2:g.12717406A>C GRCh38
NC_000012.11:g.12870340A>C , CM000674.1:g.12870340A>C GRCh37
NC_000012.10:g.12761607A>C NCBI36
NG_016341.1:g.5039A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.-434A>C (CDKN1B) ENSP00000507272.1:n.-434A>C
ENST00000682620.1:n.1631-1419A>C (CDKN1B)
ENST00000684771.1:n.585-1419A>C (CDKN1B)
ENST00000228872.9:c.-434A>C (CDKN1B) MANE Select ENSP00000228872.4:n.-434A>C
ENST00000228872.8:c.-434A>C (CDKN1B) ENSP00000228872.4:n.-434A>C
ENST00000477087.1:n.155-1419A>C (CDKN1B)
NM_004064.4:c.-434A>C (CDKN1B) NP_004055.1:n.-434A>C
XM_011520623.3:c.-1900T>G (GPR19) XP_011518925.1:n.-1900T>G
XM_017019216.2:c.-1928T>G (GPR19) XP_016874705.1:n.-1928T>G
NM_004064.5:c.-434A>C (CDKN1B) MANE Select NP_004055.1:n.-434A>C