Canonical Allele Identifier: CA493393962

Gene: CREBBP

Linked Data

• dbSNP Id: rs1475335310
• MyVariant Identifiers: chr16:g.3779006G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729005G>C , CM000678.2:g.3729005G>C	GRCh38
NC_000016.9:g.3779006G>C , CM000678.1:g.3779006G>C	GRCh37
NC_000016.8:g.3719007G>C	NCBI36
NG_009873.1:g.156116C>G
NG_009873.2:g.156709C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6042C>G MANE Select	ENSP00000262367.5:p.Pro2014=
ENST00000262367.9:c.6042C>G	ENSP00000262367.5:p.Pro2014=
ENST00000382070.7:c.5928C>G	ENSP00000371502.3:p.Pro1976=
NM_001079846.1:c.5928C>G	NP_001073315.1:p.Pro1976=
NM_004380.2:c.6042C>G	NP_004371.2:p.Pro2014=
XM_005255124.3:c.5997C>G	XP_005255181.1:p.Pro1999=
XM_005255125.3:c.5625C>G	XP_005255182.1:p.Pro1875=
XM_006720848.2:c.5781C>G	XP_006720911.1:p.Pro1927=
XM_011522380.1:c.5988C>G	XP_011520682.1:p.Pro1996=
XM_011522381.1:c.5289C>G	XP_011520683.1:p.Pro1763=
XM_005255124.4:c.5997C>G	XP_005255181.1:p.Pro1999=
XM_005255125.4:c.5625C>G	XP_005255182.1:p.Pro1875=
XM_006720848.3:c.5781C>G	XP_006720911.1:p.Pro1927=
XM_011522381.2:c.5289C>G	XP_011520683.1:p.Pro1763=
XM_017022944.1:c.6036C>G	XP_016878433.1:p.Pro2012=
NM_004380.3:c.6042C>G MANE Select	NP_004371.2:p.Pro2014=