Canonical Allele Identifier: CA276982937

Gene: CREBBP

Linked Data

• dbSNP Id: rs554111268
• gnomAD v3: 16-3740231-A-G
• gnomAD v4: 16-3740231-A-G
• MyVariant Identifiers: chr16:g.3790232A>G (hg19) ; chr16:g.3740231A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3740231A>G , CM000678.2:g.3740231A>G	GRCh38
NC_000016.9:g.3790232A>G , CM000678.1:g.3790232A>G	GRCh37
NC_000016.8:g.3730233A>G	NCBI36
NG_009873.1:g.144890T>C
NG_009873.2:g.145483T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.4133+168T>C MANE Select	ENSP00000262367.5:n.4133+168T>C
ENST00000262367.9:c.4133+168T>C	ENSP00000262367.5:n.4133+168T>C
ENST00000382070.7:c.4019+168T>C	ENSP00000371502.3:n.4019+168T>C
ENST00000570939.2:c.2768+168T>C	ENSP00000461002.2:n.2768+168T>C
ENST00000573517.6:c.439+168T>C
ENST00000574740.1:n.215+168T>C
ENST00000576720.1:n.3070+168T>C
NM_001079846.1:c.4019+168T>C	NP_001073315.1:n.4019+168T>C
NM_004380.2:c.4133+168T>C	NP_004371.2:n.4133+168T>C
XM_005255124.3:c.4088+168T>C	XP_005255181.1:n.4088+168T>C
XM_005255125.3:c.3716+168T>C	XP_005255182.1:n.3716+168T>C
XM_006720848.2:c.4133+168T>C	XP_006720911.1:n.4133+168T>C
XM_011522380.1:c.4079+168T>C	XP_011520682.1:n.4079+168T>C
XM_011522381.1:c.3380+168T>C	XP_011520683.1:n.3380+168T>C
XM_005255124.4:c.4088+168T>C	XP_005255181.1:n.4088+168T>C
XM_005255125.4:c.3716+168T>C	XP_005255182.1:n.3716+168T>C
XM_006720848.3:c.4133+168T>C	XP_006720911.1:n.4133+168T>C
XM_011522381.2:c.3380+168T>C	XP_011520683.1:n.3380+168T>C
XM_017022944.1:c.4127+168T>C	XP_016878433.1:n.4127+168T>C
NM_004380.3:c.4133+168T>C MANE Select	NP_004371.2:n.4133+168T>C