Canonical Allele Identifier: CA7869238

Gene: CREBBP

Linked Data

• dbSNP Id: rs754336198
• ExAC: 16:3779207 G / C
• gnomAD v2: 16-3779207-G-C
• gnomAD v4: 16-3729206-G-C
• MyVariant Identifiers: chr16:g.3779207G>C (hg19) ; chr16:g.3729206G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729206G>C , CM000678.2:g.3729206G>C	GRCh38
NC_000016.9:g.3779207G>C , CM000678.1:g.3779207G>C	GRCh37
NC_000016.8:g.3719208G>C	NCBI36
NG_009873.1:g.155915C>G
NG_009873.2:g.156508C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000262367.10:c.5841C>G MANE Select	ENSP00000262367.5:p.Pro1947=
ENST00000262367.9:c.5841C>G	ENSP00000262367.5:p.Pro1947=
ENST00000382070.7:c.5727C>G	ENSP00000371502.3:p.Pro1909=
NM_001079846.1:c.5727C>G	NP_001073315.1:p.Pro1909=
NM_004380.2:c.5841C>G	NP_004371.2:p.Pro1947=
XM_005255124.3:c.5796C>G	XP_005255181.1:p.Pro1932=
XM_005255125.3:c.5424C>G	XP_005255182.1:p.Pro1808=
XM_006720848.2:c.5580C>G	XP_006720911.1:p.Pro1860=
XM_011522380.1:c.5787C>G	XP_011520682.1:p.Pro1929=
XM_011522381.1:c.5088C>G	XP_011520683.1:p.Pro1696=
XM_005255124.4:c.5796C>G	XP_005255181.1:p.Pro1932=
XM_005255125.4:c.5424C>G	XP_005255182.1:p.Pro1808=
XM_006720848.3:c.5580C>G	XP_006720911.1:p.Pro1860=
XM_011522381.2:c.5088C>G	XP_011520683.1:p.Pro1696=
XM_017022944.1:c.5835C>G	XP_016878433.1:p.Pro1945=
NM_004380.3:c.5841C>G MANE Select	NP_004371.2:p.Pro1947=