Canonical Allele Identifier: CA7870289

Gene: CREBBP

Linked Data

• ClinVar Variation Id: 2957133
• ClinVar RCV Id: RCV003818820
• dbSNP Id: rs763996233
• ExAC: 16:3828069 G / T
• gnomAD v2: 16-3828069-G-T
• gnomAD v4: 16-3778068-G-T
• MyVariant Identifiers: chr16:g.3828069G>T (hg19) ; chr16:g.3778068G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3778068G>T , CM000678.2:g.3778068G>T	GRCh38
NC_000016.9:g.3828069G>T , CM000678.1:g.3828069G>T	GRCh37
NC_000016.8:g.3768070G>T	NCBI36
NG_009873.1:g.107053C>A
NG_009873.2:g.107646C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.2056C>A MANE Select	ENSP00000262367.5:p.Pro686Thr
ENST00000262367.9:c.2056C>A	ENSP00000262367.5:p.Pro686Thr
ENST00000382070.7:c.1942C>A	ENSP00000371502.3:p.Pro648Thr
ENST00000570939.2:c.661C>A	ENSP00000461002.2:p.Pro221Thr
ENST00000571826.5:c.105C>A
ENST00000572134.1:c.369C>A
ENST00000634839.1:n.218C>A
NM_001079846.1:c.1942C>A	NP_001073315.1:p.Pro648Thr
NM_004380.2:c.2056C>A	NP_004371.2:p.Pro686Thr
XM_005255124.3:c.2056C>A	XP_005255181.1:p.Pro686Thr
XM_005255125.3:c.2056C>A	XP_005255182.1:p.Pro686Thr
XM_006720848.2:c.2056C>A	XP_006720911.1:p.Pro686Thr
XM_011522380.1:c.2002C>A	XP_011520682.1:p.Pro668Thr
XM_011522381.1:c.1303C>A	XP_011520683.1:p.Pro435Thr
XM_011522382.1:c.2056C>A	XP_011520684.1:p.Pro686Thr
XM_005255124.4:c.2056C>A	XP_005255181.1:p.Pro686Thr
XM_005255125.4:c.2056C>A	XP_005255182.1:p.Pro686Thr
XM_006720848.3:c.2056C>A	XP_006720911.1:p.Pro686Thr
XM_011522381.2:c.1303C>A	XP_011520683.1:p.Pro435Thr
XM_011522382.3:c.2056C>A	XP_011520684.1:p.Pro686Thr
XM_017022944.1:c.2056C>A	XP_016878433.1:p.Pro686Thr
NM_004380.3:c.2056C>A MANE Select	NP_004371.2:p.Pro686Thr