Canonical Allele Identifier: CA394551066

Gene: CREBBP

Linked Data

• dbSNP Id: rs587778215
• MyVariant Identifiers: chr16:g.3778092T>C (hg19) ; chr16:g.3728091T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728091T>C , CM000678.2:g.3728091T>C	GRCh38
NC_000016.9:g.3778092T>C , CM000678.1:g.3778092T>C	GRCh37
NC_000016.8:g.3718093T>C	NCBI36
NG_009873.1:g.157030A>G
NG_009873.2:g.157623A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6956A>G MANE Select	ENSP00000262367.5:p.His2319Arg
ENST00000262367.9:c.6956A>G	ENSP00000262367.5:p.His2319Arg
ENST00000382070.7:c.6842A>G	ENSP00000371502.3:p.His2281Arg
NM_001079846.1:c.6842A>G	NP_001073315.1:p.His2281Arg
NM_004380.2:c.6956A>G	NP_004371.2:p.His2319Arg
XM_005255124.3:c.6911A>G	XP_005255181.1:p.His2304Arg
XM_005255125.3:c.6539A>G	XP_005255182.1:p.His2180Arg
XM_006720848.2:c.6695A>G	XP_006720911.1:p.His2232Arg
XM_011522380.1:c.6902A>G	XP_011520682.1:p.His2301Arg
XM_011522381.1:c.6203A>G	XP_011520683.1:p.His2068Arg
XM_005255124.4:c.6911A>G	XP_005255181.1:p.His2304Arg
XM_005255125.4:c.6539A>G	XP_005255182.1:p.His2180Arg
XM_006720848.3:c.6695A>G	XP_006720911.1:p.His2232Arg
XM_011522381.2:c.6203A>G	XP_011520683.1:p.His2068Arg
XM_017022944.1:c.6950A>G	XP_016878433.1:p.His2317Arg
NM_004380.3:c.6956A>G MANE Select	NP_004371.2:p.His2319Arg