Canonical Allele Identifier: CA394550260

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151298435
• MyVariant Identifiers: chr16:g.3777820G>T (hg19) ; chr16:g.3727819G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3727819G>T , CM000678.2:g.3727819G>T	GRCh38
NC_000016.9:g.3777820G>T , CM000678.1:g.3777820G>T	GRCh37
NC_000016.8:g.3717821G>T	NCBI36
NG_009873.1:g.157302C>A
NG_009873.2:g.157895C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.7228C>A MANE Select	ENSP00000262367.5:p.Pro2410Thr
ENST00000262367.9:c.7228C>A	ENSP00000262367.5:p.Pro2410Thr
ENST00000382070.7:c.7114C>A	ENSP00000371502.3:p.Pro2372Thr
NM_001079846.1:c.7114C>A	NP_001073315.1:p.Pro2372Thr
NM_004380.2:c.7228C>A	NP_004371.2:p.Pro2410Thr
XM_005255124.3:c.7183C>A	XP_005255181.1:p.Pro2395Thr
XM_005255125.3:c.6811C>A	XP_005255182.1:p.Pro2271Thr
XM_006720848.2:c.6967C>A	XP_006720911.1:p.Pro2323Thr
XM_011522380.1:c.7174C>A	XP_011520682.1:p.Pro2392Thr
XM_011522381.1:c.6475C>A	XP_011520683.1:p.Pro2159Thr
XM_005255124.4:c.7183C>A	XP_005255181.1:p.Pro2395Thr
XM_005255125.4:c.6811C>A	XP_005255182.1:p.Pro2271Thr
XM_006720848.3:c.6967C>A	XP_006720911.1:p.Pro2323Thr
XM_011522381.2:c.6475C>A	XP_011520683.1:p.Pro2159Thr
XM_017022944.1:c.7222C>A	XP_016878433.1:p.Pro2408Thr
NM_004380.3:c.7228C>A MANE Select	NP_004371.2:p.Pro2410Thr