Canonical Allele Identifier: CA394550089

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151297868
• MyVariant Identifiers: chr16:g.3777735A>T (hg19) ; chr16:g.3727734A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3727734A>T , CM000678.2:g.3727734A>T	GRCh38
NC_000016.9:g.3777735A>T , CM000678.1:g.3777735A>T	GRCh37
NC_000016.8:g.3717736A>T	NCBI36
NG_009873.1:g.157387T>A
NG_009873.2:g.157980T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.7313T>A MANE Select	ENSP00000262367.5:p.Phe2438Tyr
ENST00000262367.9:c.7313T>A	ENSP00000262367.5:p.Phe2438Tyr
ENST00000382070.7:c.7199T>A	ENSP00000371502.3:p.Phe2400Tyr
NM_001079846.1:c.7199T>A	NP_001073315.1:p.Phe2400Tyr
NM_004380.2:c.7313T>A	NP_004371.2:p.Phe2438Tyr
XM_005255124.3:c.7268T>A	XP_005255181.1:p.Phe2423Tyr
XM_005255125.3:c.6896T>A	XP_005255182.1:p.Phe2299Tyr
XM_006720848.2:c.7052T>A	XP_006720911.1:p.Phe2351Tyr
XM_011522380.1:c.7259T>A	XP_011520682.1:p.Phe2420Tyr
XM_011522381.1:c.6560T>A	XP_011520683.1:p.Phe2187Tyr
XM_005255124.4:c.7268T>A	XP_005255181.1:p.Phe2423Tyr
XM_005255125.4:c.6896T>A	XP_005255182.1:p.Phe2299Tyr
XM_006720848.3:c.7052T>A	XP_006720911.1:p.Phe2351Tyr
XM_011522381.2:c.6560T>A	XP_011520683.1:p.Phe2187Tyr
XM_017022944.1:c.7307T>A	XP_016878433.1:p.Phe2436Tyr
NM_004380.3:c.7313T>A MANE Select	NP_004371.2:p.Phe2438Tyr