Canonical Allele Identifier: CA394550537

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151299282
• MyVariant Identifiers: chr16:g.3777949T>C (hg19) ; chr16:g.3727948T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3727948T>C , CM000678.2:g.3727948T>C	GRCh38
NC_000016.9:g.3777949T>C , CM000678.1:g.3777949T>C	GRCh37
NC_000016.8:g.3717950T>C	NCBI36
NG_009873.1:g.157173A>G
NG_009873.2:g.157766A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.7099A>G MANE Select	ENSP00000262367.5:p.Ile2367Val
ENST00000262367.9:c.7099A>G	ENSP00000262367.5:p.Ile2367Val
ENST00000382070.7:c.6985A>G	ENSP00000371502.3:p.Ile2329Val
NM_001079846.1:c.6985A>G	NP_001073315.1:p.Ile2329Val
NM_004380.2:c.7099A>G	NP_004371.2:p.Ile2367Val
XM_005255124.3:c.7054A>G	XP_005255181.1:p.Ile2352Val
XM_005255125.3:c.6682A>G	XP_005255182.1:p.Ile2228Val
XM_006720848.2:c.6838A>G	XP_006720911.1:p.Ile2280Val
XM_011522380.1:c.7045A>G	XP_011520682.1:p.Ile2349Val
XM_011522381.1:c.6346A>G	XP_011520683.1:p.Ile2116Val
XM_005255124.4:c.7054A>G	XP_005255181.1:p.Ile2352Val
XM_005255125.4:c.6682A>G	XP_005255182.1:p.Ile2228Val
XM_006720848.3:c.6838A>G	XP_006720911.1:p.Ile2280Val
XM_011522381.2:c.6346A>G	XP_011520683.1:p.Ile2116Val
XM_017022944.1:c.7093A>G	XP_016878433.1:p.Ile2365Val
NM_004380.3:c.7099A>G MANE Select	NP_004371.2:p.Ile2367Val