Canonical Allele Identifier: CA2617685010

Gene: CDKN1B GPR19

Linked Data

• gnomAD v4: 12-12717394-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.12717394C>A , CM000674.2:g.12717394C>A	GRCh38
NC_000012.11:g.12870328C>A , CM000674.1:g.12870328C>A	GRCh37
NC_000012.10:g.12761595C>A	NCBI36
NG_016341.1:g.5027C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614874.2:c.-446C>A (CDKN1B)	ENSP00000507272.1:n.-446C>A
ENST00000682620.1:n.1631-1431C>A (CDKN1B)
ENST00000684771.1:n.585-1431C>A (CDKN1B)
ENST00000228872.9:c.-446C>A (CDKN1B) MANE Select	ENSP00000228872.4:n.-446C>A
ENST00000228872.8:c.-446C>A (CDKN1B)	ENSP00000228872.4:n.-446C>A
ENST00000477087.1:n.155-1431C>A (CDKN1B)
NM_004064.4:c.-446C>A (CDKN1B)	NP_004055.1:n.-446C>A
XM_011520623.3:c.-1888G>T (GPR19)	XP_011518925.1:n.-1888G>T
XM_017019216.2:c.-1916G>T (GPR19)	XP_016874705.1:n.-1916G>T
NM_004064.5:c.-446C>A (CDKN1B) MANE Select	NP_004055.1:n.-446C>A