Canonical Allele Identifier: CA944839969

Gene: CDKN1B GPR19

Linked Data

• dbSNP Id: rs1946482759
• gnomAD v3: 12-12717749-AGG-A
• gnomAD v4: 12-12717749-AGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12717752_12717753del , CM000674.2:g.12717752_12717753del	GRCh38
NC_000012.11:g.12870686_12870687del , CM000674.1:g.12870686_12870687del	GRCh37
NC_000012.10:g.12761953_12761954del	NCBI36
NG_016341.1:g.5385_5386del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614874.2:c.-88_-87del (CDKN1B)	ENSP00000507272.1:n.-88_-87del
ENST00000682620.1:n.1631-1073_1631-1072del (CDKN1B)
ENST00000684771.1:n.585-1073_585-1072del (CDKN1B)
ENST00000228872.9:c.-88_-87del (CDKN1B) MANE Select	ENSP00000228872.4:n.-88_-87del
ENST00000228872.8:c.-88_-87del (CDKN1B)	ENSP00000228872.4:n.-88_-87del
ENST00000477087.1:n.155-1073_155-1072del (CDKN1B)
NM_004064.4:c.-88_-87del (CDKN1B)	NP_004055.1:n.-88_-87del
XM_011520623.3:c.-2245_-2244del (GPR19)	XP_011518925.1:n.-2245_-2244del
XM_017019216.2:c.-2273_-2272del (GPR19)	XP_016874705.1:n.-2273_-2272del
NM_004064.5:c.-88_-87del (CDKN1B) MANE Select	NP_004055.1:n.-88_-87del