Canonical Allele Identifier: CA493393761

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151305781
• MyVariant Identifiers: chr16:g.3778886G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728885G>C , CM000678.2:g.3728885G>C	GRCh38
NC_000016.9:g.3778886G>C , CM000678.1:g.3778886G>C	GRCh37
NC_000016.8:g.3718887G>C	NCBI36
NG_009873.1:g.156236C>G
NG_009873.2:g.156829C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6162C>G MANE Select	ENSP00000262367.5:p.Pro2054=
ENST00000262367.9:c.6162C>G	ENSP00000262367.5:p.Pro2054=
ENST00000382070.7:c.6048C>G	ENSP00000371502.3:p.Pro2016=
NM_001079846.1:c.6048C>G	NP_001073315.1:p.Pro2016=
NM_004380.2:c.6162C>G	NP_004371.2:p.Pro2054=
XM_005255124.3:c.6117C>G	XP_005255181.1:p.Pro2039=
XM_005255125.3:c.5745C>G	XP_005255182.1:p.Pro1915=
XM_006720848.2:c.5901C>G	XP_006720911.1:p.Pro1967=
XM_011522380.1:c.6108C>G	XP_011520682.1:p.Pro2036=
XM_011522381.1:c.5409C>G	XP_011520683.1:p.Pro1803=
XM_005255124.4:c.6117C>G	XP_005255181.1:p.Pro2039=
XM_005255125.4:c.5745C>G	XP_005255182.1:p.Pro1915=
XM_006720848.3:c.5901C>G	XP_006720911.1:p.Pro1967=
XM_011522381.2:c.5409C>G	XP_011520683.1:p.Pro1803=
XM_017022944.1:c.6156C>G	XP_016878433.1:p.Pro2052=
NM_004380.3:c.6162C>G MANE Select	NP_004371.2:p.Pro2054=