Canonical Allele Identifier: CA493393510

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151300007
• MyVariant Identifiers: chr16:g.3778061A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728060A>G , CM000678.2:g.3728060A>G	GRCh38
NC_000016.9:g.3778061A>G , CM000678.1:g.3778061A>G	GRCh37
NC_000016.8:g.3718062A>G	NCBI36
NG_009873.1:g.157061T>C
NG_009873.2:g.157654T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6987T>C MANE Select	ENSP00000262367.5:p.His2329=
ENST00000262367.9:c.6987T>C	ENSP00000262367.5:p.His2329=
ENST00000382070.7:c.6873T>C	ENSP00000371502.3:p.His2291=
NM_001079846.1:c.6873T>C	NP_001073315.1:p.His2291=
NM_004380.2:c.6987T>C	NP_004371.2:p.His2329=
XM_005255124.3:c.6942T>C	XP_005255181.1:p.His2314=
XM_005255125.3:c.6570T>C	XP_005255182.1:p.His2190=
XM_006720848.2:c.6726T>C	XP_006720911.1:p.His2242=
XM_011522380.1:c.6933T>C	XP_011520682.1:p.His2311=
XM_011522381.1:c.6234T>C	XP_011520683.1:p.His2078=
XM_005255124.4:c.6942T>C	XP_005255181.1:p.His2314=
XM_005255125.4:c.6570T>C	XP_005255182.1:p.His2190=
XM_006720848.3:c.6726T>C	XP_006720911.1:p.His2242=
XM_011522381.2:c.6234T>C	XP_011520683.1:p.His2078=
XM_017022944.1:c.6981T>C	XP_016878433.1:p.His2327=
NM_004380.3:c.6987T>C MANE Select	NP_004371.2:p.His2329=