Canonical Allele Identifier: CA2617685230

Gene: CDKN1B GPR19

Linked Data

• gnomAD v4: 12-12717617-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12717617T>C , CM000674.2:g.12717617T>C	GRCh38
NC_000012.11:g.12870551T>C , CM000674.1:g.12870551T>C	GRCh37
NC_000012.10:g.12761818T>C	NCBI36
NG_016341.1:g.5250T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614874.2:c.-223T>C (CDKN1B)	ENSP00000507272.1:n.-223T>C
ENST00000682620.1:n.1631-1208T>C (CDKN1B)
ENST00000684771.1:n.585-1208T>C (CDKN1B)
ENST00000228872.9:c.-223T>C (CDKN1B) MANE Select	ENSP00000228872.4:n.-223T>C
ENST00000228872.8:c.-223T>C (CDKN1B)	ENSP00000228872.4:n.-223T>C
ENST00000477087.1:n.155-1208T>C (CDKN1B)
NM_004064.4:c.-223T>C (CDKN1B)	NP_004055.1:n.-223T>C
XM_011520623.3:c.-2111A>G (GPR19)	XP_011518925.1:n.-2111A>G
XM_017019216.2:c.-2139A>G (GPR19)	XP_016874705.1:n.-2139A>G
NM_004064.5:c.-223T>C (CDKN1B) MANE Select	NP_004055.1:n.-223T>C