Canonical Allele Identifier: CA394557827

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151312760
• MyVariant Identifiers: chr16:g.3779871T>C (hg19) ; chr16:g.3729870T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729870T>C , CM000678.2:g.3729870T>C	GRCh38
NC_000016.9:g.3779871T>C , CM000678.1:g.3779871T>C	GRCh37
NC_000016.8:g.3719872T>C	NCBI36
NG_009873.1:g.155251A>G
NG_009873.2:g.155844A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5177A>G MANE Select	ENSP00000262367.5:p.Tyr1726Cys
ENST00000262367.9:c.5177A>G	ENSP00000262367.5:p.Tyr1726Cys
ENST00000382070.7:c.5063A>G	ENSP00000371502.3:p.Tyr1688Cys
NM_001079846.1:c.5063A>G	NP_001073315.1:p.Tyr1688Cys
NM_004380.2:c.5177A>G	NP_004371.2:p.Tyr1726Cys
XM_005255124.3:c.5132A>G	XP_005255181.1:p.Tyr1711Cys
XM_005255125.3:c.4760A>G	XP_005255182.1:p.Tyr1587Cys
XM_006720848.2:c.4916A>G	XP_006720911.1:p.Tyr1639Cys
XM_011522380.1:c.5123A>G	XP_011520682.1:p.Tyr1708Cys
XM_011522381.1:c.4424A>G	XP_011520683.1:p.Tyr1475Cys
XM_005255124.4:c.5132A>G	XP_005255181.1:p.Tyr1711Cys
XM_005255125.4:c.4760A>G	XP_005255182.1:p.Tyr1587Cys
XM_006720848.3:c.4916A>G	XP_006720911.1:p.Tyr1639Cys
XM_011522381.2:c.4424A>G	XP_011520683.1:p.Tyr1475Cys
XM_017022944.1:c.5171A>G	XP_016878433.1:p.Tyr1724Cys
NM_004380.3:c.5177A>G MANE Select	NP_004371.2:p.Tyr1726Cys