Canonical Allele Identifier: CA493394031

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151309809
• MyVariant Identifiers: chr16:g.3779474G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729473G>A , CM000678.2:g.3729473G>A	GRCh38
NC_000016.9:g.3779474G>A , CM000678.1:g.3779474G>A	GRCh37
NC_000016.8:g.3719475G>A	NCBI36
NG_009873.1:g.155648C>T
NG_009873.2:g.156241C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5574C>T MANE Select	ENSP00000262367.5:p.Arg1858=
ENST00000262367.9:c.5574C>T	ENSP00000262367.5:p.Arg1858=
ENST00000382070.7:c.5460C>T	ENSP00000371502.3:p.Arg1820=
NM_001079846.1:c.5460C>T	NP_001073315.1:p.Arg1820=
NM_004380.2:c.5574C>T	NP_004371.2:p.Arg1858=
XM_005255124.3:c.5529C>T	XP_005255181.1:p.Arg1843=
XM_005255125.3:c.5157C>T	XP_005255182.1:p.Arg1719=
XM_006720848.2:c.5313C>T	XP_006720911.1:p.Arg1771=
XM_011522380.1:c.5520C>T	XP_011520682.1:p.Arg1840=
XM_011522381.1:c.4821C>T	XP_011520683.1:p.Arg1607=
XM_005255124.4:c.5529C>T	XP_005255181.1:p.Arg1843=
XM_005255125.4:c.5157C>T	XP_005255182.1:p.Arg1719=
XM_006720848.3:c.5313C>T	XP_006720911.1:p.Arg1771=
XM_011522381.2:c.4821C>T	XP_011520683.1:p.Arg1607=
XM_017022944.1:c.5568C>T	XP_016878433.1:p.Arg1856=
NM_004380.3:c.5574C>T MANE Select	NP_004371.2:p.Arg1858=