Canonical Allele Identifier: CA493394368

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151310751
• MyVariant Identifiers: chr16:g.3779603G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729602G>T , CM000678.2:g.3729602G>T	GRCh38
NC_000016.9:g.3779603G>T , CM000678.1:g.3779603G>T	GRCh37
NC_000016.8:g.3719604G>T	NCBI36
NG_009873.1:g.155519C>A
NG_009873.2:g.156112C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5445C>A MANE Select	ENSP00000262367.5:p.Gly1815=
ENST00000262367.9:c.5445C>A	ENSP00000262367.5:p.Gly1815=
ENST00000382070.7:c.5331C>A	ENSP00000371502.3:p.Gly1777=
NM_001079846.1:c.5331C>A	NP_001073315.1:p.Gly1777=
NM_004380.2:c.5445C>A	NP_004371.2:p.Gly1815=
XM_005255124.3:c.5400C>A	XP_005255181.1:p.Gly1800=
XM_005255125.3:c.5028C>A	XP_005255182.1:p.Gly1676=
XM_006720848.2:c.5184C>A	XP_006720911.1:p.Gly1728=
XM_011522380.1:c.5391C>A	XP_011520682.1:p.Gly1797=
XM_011522381.1:c.4692C>A	XP_011520683.1:p.Gly1564=
XM_005255124.4:c.5400C>A	XP_005255181.1:p.Gly1800=
XM_005255125.4:c.5028C>A	XP_005255182.1:p.Gly1676=
XM_006720848.3:c.5184C>A	XP_006720911.1:p.Gly1728=
XM_011522381.2:c.4692C>A	XP_011520683.1:p.Gly1564=
XM_017022944.1:c.5439C>A	XP_016878433.1:p.Gly1813=
NM_004380.3:c.5445C>A MANE Select	NP_004371.2:p.Gly1815=