Canonical Allele Identifier: CA394555117

Gene: CREBBP

Linked Data

• dbSNP Id: rs772270271
• gnomAD v2: 16-3779170-G-A
• gnomAD v4: 16-3729169-G-A
• MyVariant Identifiers: chr16:g.3779170G>A (hg19) ; chr16:g.3729169G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729169G>A , CM000678.2:g.3729169G>A	GRCh38
NC_000016.9:g.3779170G>A , CM000678.1:g.3779170G>A	GRCh37
NC_000016.8:g.3719171G>A	NCBI36
NG_009873.1:g.155952C>T
NG_009873.2:g.156545C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5878C>T MANE Select	ENSP00000262367.5:p.Arg1960Trp
ENST00000262367.9:c.5878C>T	ENSP00000262367.5:p.Arg1960Trp
ENST00000382070.7:c.5764C>T	ENSP00000371502.3:p.Arg1922Trp
NM_001079846.1:c.5764C>T	NP_001073315.1:p.Arg1922Trp
NM_004380.2:c.5878C>T	NP_004371.2:p.Arg1960Trp
XM_005255124.3:c.5833C>T	XP_005255181.1:p.Arg1945Trp
XM_005255125.3:c.5461C>T	XP_005255182.1:p.Arg1821Trp
XM_006720848.2:c.5617C>T	XP_006720911.1:p.Arg1873Trp
XM_011522380.1:c.5824C>T	XP_011520682.1:p.Arg1942Trp
XM_011522381.1:c.5125C>T	XP_011520683.1:p.Arg1709Trp
XM_005255124.4:c.5833C>T	XP_005255181.1:p.Arg1945Trp
XM_005255125.4:c.5461C>T	XP_005255182.1:p.Arg1821Trp
XM_006720848.3:c.5617C>T	XP_006720911.1:p.Arg1873Trp
XM_011522381.2:c.5125C>T	XP_011520683.1:p.Arg1709Trp
XM_017022944.1:c.5872C>T	XP_016878433.1:p.Arg1958Trp
NM_004380.3:c.5878C>T MANE Select	NP_004371.2:p.Arg1960Trp