Canonical Allele Identifier: CA2017047116
Gene: CDKN1B HGNC NCBI
GPR19 HGNC NCBI

Linked Data

dbSNP Id: rs1946474237

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12717399T>C , CM000674.2:g.12717399T>C GRCh38
NC_000012.11:g.12870333T>C , CM000674.1:g.12870333T>C GRCh37
NC_000012.10:g.12761600T>C NCBI36
NG_016341.1:g.5032T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000614874.2:c.-441T>C (CDKN1B) ENSP00000507272.1:n.-441T>C
ENST00000682620.1:n.1631-1426T>C (CDKN1B)
ENST00000684771.1:n.585-1426T>C (CDKN1B)
ENST00000228872.9:c.-441T>C (CDKN1B) MANE Select ENSP00000228872.4:n.-441T>C
ENST00000228872.8:c.-441T>C (CDKN1B) ENSP00000228872.4:n.-441T>C
ENST00000477087.1:n.155-1426T>C (CDKN1B)
NM_004064.4:c.-441T>C (CDKN1B) NP_004055.1:n.-441T>C
XM_011520623.3:c.-1893A>G (GPR19) XP_011518925.1:n.-1893A>G
XM_017019216.2:c.-1921A>G (GPR19) XP_016874705.1:n.-1921A>G
NM_004064.5:c.-441T>C (CDKN1B) MANE Select NP_004055.1:n.-441T>C