Canonical Allele Identifier: CA10632230

Gene: CDKN1B GPR19

Linked Data

• ClinVar Variation Id: 307655
• ClinVar RCV Id: RCV000309141
• dbSNP Id: rs561344485
• gnomAD v3: 12-12717586-C-G
• gnomAD v4: 12-12717586-C-G
• MyVariant Identifiers: chr12:g.12870520C>G (hg19) ; chr12:g.12717586C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12717586C>G , CM000674.2:g.12717586C>G	GRCh38
NC_000012.11:g.12870520C>G , CM000674.1:g.12870520C>G	GRCh37
NC_000012.10:g.12761787C>G	NCBI36
NG_016341.1:g.5219C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614874.2:c.-254C>G (CDKN1B)	ENSP00000507272.1:n.-254C>G
ENST00000682620.1:n.1631-1239C>G (CDKN1B)
ENST00000684771.1:n.585-1239C>G (CDKN1B)
ENST00000228872.9:c.-254C>G (CDKN1B) MANE Select	ENSP00000228872.4:n.-254C>G
ENST00000228872.8:c.-254C>G (CDKN1B)	ENSP00000228872.4:n.-254C>G
ENST00000477087.1:n.155-1239C>G (CDKN1B)
NM_004064.4:c.-254C>G (CDKN1B)	NP_004055.1:n.-254C>G
XM_011520623.3:c.-2080G>C (GPR19)	XP_011518925.1:n.-2080G>C
XM_017019216.2:c.-2108G>C (GPR19)	XP_016874705.1:n.-2108G>C
NM_004064.5:c.-254C>G (CDKN1B) MANE Select	NP_004055.1:n.-254C>G