Canonical Allele Identifier: CA10641335
Gene: CDKN1B HGNC NCBI
GPR19 HGNC NCBI

Linked Data

ClinVar Variation Id: 307658
dbSNP Id: rs34330

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.12717761T>C , CM000674.2:g.12717761T>C GRCh38
NC_000012.11:g.12870695T>C , CM000674.1:g.12870695T>C GRCh37
NC_000012.10:g.12761962T>C NCBI36
NG_016341.1:g.5394T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000228872.9:c.-79T>C MANE Select ENSP00000228872.4:p.=
ENST00000228872.8:c.-79T>C ENSP00000228872.4:p.=
ENST00000477087.1:n.155-1064T>C
NM_004064.4:c.-79T>C (CDKN1B) NP_004055.1:p.=
XM_011520623.3:c.-2255A>G (GPR19) XP_011518925.1:p.=
XM_017019216.2:c.-2283A>G (GPR19) XP_016874705.1:p.=
NM_004064.5:c.-79T>C (CDKN1B) MANE Select NP_004055.1:p.=