Canonical Allele Identifier: CA394550864

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151299909
• MyVariant Identifiers: chr16:g.3778045T>C (hg19) ; chr16:g.3728044T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728044T>C , CM000678.2:g.3728044T>C	GRCh38
NC_000016.9:g.3778045T>C , CM000678.1:g.3778045T>C	GRCh37
NC_000016.8:g.3718046T>C	NCBI36
NG_009873.1:g.157077A>G
NG_009873.2:g.157670A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.7003A>G MANE Select	ENSP00000262367.5:p.Ile2335Val
ENST00000262367.9:c.7003A>G	ENSP00000262367.5:p.Ile2335Val
ENST00000382070.7:c.6889A>G	ENSP00000371502.3:p.Ile2297Val
NM_001079846.1:c.6889A>G	NP_001073315.1:p.Ile2297Val
NM_004380.2:c.7003A>G	NP_004371.2:p.Ile2335Val
XM_005255124.3:c.6958A>G	XP_005255181.1:p.Ile2320Val
XM_005255125.3:c.6586A>G	XP_005255182.1:p.Ile2196Val
XM_006720848.2:c.6742A>G	XP_006720911.1:p.Ile2248Val
XM_011522380.1:c.6949A>G	XP_011520682.1:p.Ile2317Val
XM_011522381.1:c.6250A>G	XP_011520683.1:p.Ile2084Val
XM_005255124.4:c.6958A>G	XP_005255181.1:p.Ile2320Val
XM_005255125.4:c.6586A>G	XP_005255182.1:p.Ile2196Val
XM_006720848.3:c.6742A>G	XP_006720911.1:p.Ile2248Val
XM_011522381.2:c.6250A>G	XP_011520683.1:p.Ile2084Val
XM_017022944.1:c.6997A>G	XP_016878433.1:p.Ile2333Val
NM_004380.3:c.7003A>G MANE Select	NP_004371.2:p.Ile2335Val