Canonical Allele Identifier: CA394550473

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151299093
• MyVariant Identifiers: chr16:g.3777919A>G (hg19) ; chr16:g.3727918A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3727918A>G , CM000678.2:g.3727918A>G	GRCh38
NC_000016.9:g.3777919A>G , CM000678.1:g.3777919A>G	GRCh37
NC_000016.8:g.3717920A>G	NCBI36
NG_009873.1:g.157203T>C
NG_009873.2:g.157796T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.7129T>C MANE Select	ENSP00000262367.5:p.Ser2377Pro
ENST00000262367.9:c.7129T>C	ENSP00000262367.5:p.Ser2377Pro
ENST00000382070.7:c.7015T>C	ENSP00000371502.3:p.Ser2339Pro
NM_001079846.1:c.7015T>C	NP_001073315.1:p.Ser2339Pro
NM_004380.2:c.7129T>C	NP_004371.2:p.Ser2377Pro
XM_005255124.3:c.7084T>C	XP_005255181.1:p.Ser2362Pro
XM_005255125.3:c.6712T>C	XP_005255182.1:p.Ser2238Pro
XM_006720848.2:c.6868T>C	XP_006720911.1:p.Ser2290Pro
XM_011522380.1:c.7075T>C	XP_011520682.1:p.Ser2359Pro
XM_011522381.1:c.6376T>C	XP_011520683.1:p.Ser2126Pro
XM_005255124.4:c.7084T>C	XP_005255181.1:p.Ser2362Pro
XM_005255125.4:c.6712T>C	XP_005255182.1:p.Ser2238Pro
XM_006720848.3:c.6868T>C	XP_006720911.1:p.Ser2290Pro
XM_011522381.2:c.6376T>C	XP_011520683.1:p.Ser2126Pro
XM_017022944.1:c.7123T>C	XP_016878433.1:p.Ser2375Pro
NM_004380.3:c.7129T>C MANE Select	NP_004371.2:p.Ser2377Pro