Canonical Allele Identifier: CA233058986

Gene: CDKN1B GPR19

Linked Data

• dbSNP Id: rs1012728414
• gnomAD v4: 12-12717391-C-G
• MyVariant Identifiers: chr12:g.12870325C>G (hg19) ; chr12:g.12717391C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12717391C>G , CM000674.2:g.12717391C>G	GRCh38
NC_000012.11:g.12870325C>G , CM000674.1:g.12870325C>G	GRCh37
NC_000012.10:g.12761592C>G	NCBI36
NG_016341.1:g.5024C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614874.2:c.-449C>G (CDKN1B)	ENSP00000507272.1:n.-449C>G
ENST00000682620.1:n.1631-1434C>G (CDKN1B)
ENST00000684771.1:n.585-1434C>G (CDKN1B)
ENST00000228872.9:c.-449C>G (CDKN1B) MANE Select	ENSP00000228872.4:n.-449C>G
ENST00000228872.8:c.-449C>G (CDKN1B)	ENSP00000228872.4:n.-449C>G
ENST00000477087.1:n.155-1434C>G (CDKN1B)
NM_004064.4:c.-449C>G (CDKN1B)	NP_004055.1:n.-449C>G
XM_011520623.3:c.-1885G>C (GPR19)	XP_011518925.1:n.-1885G>C
XM_017019216.2:c.-1913G>C (GPR19)	XP_016874705.1:n.-1913G>C
NM_004064.5:c.-449C>G (CDKN1B) MANE Select	NP_004055.1:n.-449C>G