Canonical Allele Identifier: CA493393034

Gene: CREBBP

Linked Data

• dbSNP Id: rs1312025473
• MyVariant Identifiers: chr16:g.3778130C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728129C>G , CM000678.2:g.3728129C>G	GRCh38
NC_000016.9:g.3778130C>G , CM000678.1:g.3778130C>G	GRCh37
NC_000016.8:g.3718131C>G	NCBI36
NG_009873.1:g.156992G>C
NG_009873.2:g.157585G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6918G>C MANE Select	ENSP00000262367.5:p.Gly2306=
ENST00000262367.9:c.6918G>C	ENSP00000262367.5:p.Gly2306=
ENST00000382070.7:c.6804G>C	ENSP00000371502.3:p.Gly2268=
NM_001079846.1:c.6804G>C	NP_001073315.1:p.Gly2268=
NM_004380.2:c.6918G>C	NP_004371.2:p.Gly2306=
XM_005255124.3:c.6873G>C	XP_005255181.1:p.Gly2291=
XM_005255125.3:c.6501G>C	XP_005255182.1:p.Gly2167=
XM_006720848.2:c.6657G>C	XP_006720911.1:p.Gly2219=
XM_011522380.1:c.6864G>C	XP_011520682.1:p.Gly2288=
XM_011522381.1:c.6165G>C	XP_011520683.1:p.Gly2055=
XM_005255124.4:c.6873G>C	XP_005255181.1:p.Gly2291=
XM_005255125.4:c.6501G>C	XP_005255182.1:p.Gly2167=
XM_006720848.3:c.6657G>C	XP_006720911.1:p.Gly2219=
XM_011522381.2:c.6165G>C	XP_011520683.1:p.Gly2055=
XM_017022944.1:c.6912G>C	XP_016878433.1:p.Gly2304=
NM_004380.3:c.6918G>C MANE Select	NP_004371.2:p.Gly2306=