Canonical Allele Identifier: CA394550532

Gene: CREBBP

Linked Data

• dbSNP Id: rs769109100
• MyVariant Identifiers: chr16:g.3777946G>C (hg19) ; chr16:g.3727945G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3727945G>C , CM000678.2:g.3727945G>C	GRCh38
NC_000016.9:g.3777946G>C , CM000678.1:g.3777946G>C	GRCh37
NC_000016.8:g.3717947G>C	NCBI36
NG_009873.1:g.157176C>G
NG_009873.2:g.157769C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.7102C>G MANE Select	ENSP00000262367.5:p.Gln2368Glu
ENST00000262367.9:c.7102C>G	ENSP00000262367.5:p.Gln2368Glu
ENST00000382070.7:c.6988C>G	ENSP00000371502.3:p.Gln2330Glu
NM_001079846.1:c.6988C>G	NP_001073315.1:p.Gln2330Glu
NM_004380.2:c.7102C>G	NP_004371.2:p.Gln2368Glu
XM_005255124.3:c.7057C>G	XP_005255181.1:p.Gln2353Glu
XM_005255125.3:c.6685C>G	XP_005255182.1:p.Gln2229Glu
XM_006720848.2:c.6841C>G	XP_006720911.1:p.Gln2281Glu
XM_011522380.1:c.7048C>G	XP_011520682.1:p.Gln2350Glu
XM_011522381.1:c.6349C>G	XP_011520683.1:p.Gln2117Glu
XM_005255124.4:c.7057C>G	XP_005255181.1:p.Gln2353Glu
XM_005255125.4:c.6685C>G	XP_005255182.1:p.Gln2229Glu
XM_006720848.3:c.6841C>G	XP_006720911.1:p.Gln2281Glu
XM_011522381.2:c.6349C>G	XP_011520683.1:p.Gln2117Glu
XM_017022944.1:c.7096C>G	XP_016878433.1:p.Gln2366Glu
NM_004380.3:c.7102C>G MANE Select	NP_004371.2:p.Gln2368Glu