Canonical Allele Identifier: CA394553765

Gene: CREBBP

Linked Data

• dbSNP Id: rs2051824806
• MyVariant Identifiers: chr16:g.3778782A>G (hg19) ; chr16:g.3728781A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728781A>G , CM000678.2:g.3728781A>G	GRCh38
NC_000016.9:g.3778782A>G , CM000678.1:g.3778782A>G	GRCh37
NC_000016.8:g.3718783A>G	NCBI36
NG_009873.1:g.156340T>C
NG_009873.2:g.156933T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6266T>C MANE Select	ENSP00000262367.5:p.Ile2089Thr
ENST00000262367.9:c.6266T>C	ENSP00000262367.5:p.Ile2089Thr
ENST00000382070.7:c.6152T>C	ENSP00000371502.3:p.Ile2051Thr
NM_001079846.1:c.6152T>C	NP_001073315.1:p.Ile2051Thr
NM_004380.2:c.6266T>C	NP_004371.2:p.Ile2089Thr
XM_005255124.3:c.6221T>C	XP_005255181.1:p.Ile2074Thr
XM_005255125.3:c.5849T>C	XP_005255182.1:p.Ile1950Thr
XM_006720848.2:c.6005T>C	XP_006720911.1:p.Ile2002Thr
XM_011522380.1:c.6212T>C	XP_011520682.1:p.Ile2071Thr
XM_011522381.1:c.5513T>C	XP_011520683.1:p.Ile1838Thr
XM_005255124.4:c.6221T>C	XP_005255181.1:p.Ile2074Thr
XM_005255125.4:c.5849T>C	XP_005255182.1:p.Ile1950Thr
XM_006720848.3:c.6005T>C	XP_006720911.1:p.Ile2002Thr
XM_011522381.2:c.5513T>C	XP_011520683.1:p.Ile1838Thr
XM_017022944.1:c.6260T>C	XP_016878433.1:p.Ile2087Thr
NM_004380.3:c.6266T>C MANE Select	NP_004371.2:p.Ile2089Thr