Canonical Allele Identifier: CA394566136

Gene: CREBBP

Linked Data

• dbSNP Id: rs989859922
• MyVariant Identifiers: chr16:g.3860743G>T (hg19) ; chr16:g.3810742G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3810742G>T , CM000678.2:g.3810742G>T	GRCh38
NC_000016.9:g.3860743G>T , CM000678.1:g.3860743G>T	GRCh37
NC_000016.8:g.3800744G>T	NCBI36
NG_009873.1:g.74379C>A
NG_009873.2:g.74972C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.836C>A MANE Select	ENSP00000262367.5:p.Pro279His
ENST00000635899.1:n.78C>A
ENST00000262367.9:c.836C>A	ENSP00000262367.5:p.Pro279His
ENST00000382070.7:c.836C>A	ENSP00000371502.3:p.Pro279His
NM_001079846.1:c.836C>A	NP_001073315.1:p.Pro279His
NM_004380.2:c.836C>A	NP_004371.2:p.Pro279His
XM_005255124.3:c.836C>A	XP_005255181.1:p.Pro279His
XM_005255125.3:c.836C>A	XP_005255182.1:p.Pro279His
XM_006720848.2:c.836C>A	XP_006720911.1:p.Pro279His
XM_011522380.1:c.782C>A	XP_011520682.1:p.Pro261His
XM_011522381.1:c.83C>A	XP_011520683.1:p.Pro28His
XM_011522382.1:c.836C>A	XP_011520684.1:p.Pro279His
XM_005255124.4:c.836C>A	XP_005255181.1:p.Pro279His
XM_005255125.4:c.836C>A	XP_005255182.1:p.Pro279His
XM_006720848.3:c.836C>A	XP_006720911.1:p.Pro279His
XM_011522381.2:c.83C>A	XP_011520683.1:p.Pro28His
XM_011522382.3:c.836C>A	XP_011520684.1:p.Pro279His
XM_017022944.1:c.836C>A	XP_016878433.1:p.Pro279His
NM_004380.3:c.836C>A MANE Select	NP_004371.2:p.Pro279His