Canonical Allele Identifier: CA684979617

Gene: CDKN1B GPR19

Linked Data

• dbSNP Id: rs1248763392
• gnomAD v3: 12-12717419-G-A
• gnomAD v4: 12-12717419-G-A
• MyVariant Identifiers: chr12:g.12870353G>A (hg19) ; chr12:g.12717419G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12717419G>A , CM000674.2:g.12717419G>A	GRCh38
NC_000012.11:g.12870353G>A , CM000674.1:g.12870353G>A	GRCh37
NC_000012.10:g.12761620G>A	NCBI36
NG_016341.1:g.5052G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614874.2:c.-421G>A (CDKN1B)	ENSP00000507272.1:n.-421G>A
ENST00000682620.1:n.1631-1406G>A (CDKN1B)
ENST00000684771.1:n.585-1406G>A (CDKN1B)
ENST00000228872.9:c.-421G>A (CDKN1B) MANE Select	ENSP00000228872.4:n.-421G>A
ENST00000228872.8:c.-421G>A (CDKN1B)	ENSP00000228872.4:n.-421G>A
ENST00000477087.1:n.155-1406G>A (CDKN1B)
NM_004064.4:c.-421G>A (CDKN1B)	NP_004055.1:n.-421G>A
XM_011520623.3:c.-1913C>T (GPR19)	XP_011518925.1:n.-1913C>T
XM_017019216.2:c.-1941C>T (GPR19)	XP_016874705.1:n.-1941C>T
NM_004064.5:c.-421G>A (CDKN1B) MANE Select	NP_004055.1:n.-421G>A