Canonical Allele Identifier: CA394555237

Gene: CREBBP

Linked Data

• dbSNP Id: rs1176184150
• gnomAD v3: 16-3729198-T-C
• gnomAD v4: 16-3729198-T-C
• MyVariant Identifiers: chr16:g.3779199T>C (hg19) ; chr16:g.3729198T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729198T>C , CM000678.2:g.3729198T>C	GRCh38
NC_000016.9:g.3779199T>C , CM000678.1:g.3779199T>C	GRCh37
NC_000016.8:g.3719200T>C	NCBI36
NG_009873.1:g.155923A>G
NG_009873.2:g.156516A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5849A>G MANE Select	ENSP00000262367.5:p.Gln1950Arg
ENST00000262367.9:c.5849A>G	ENSP00000262367.5:p.Gln1950Arg
ENST00000382070.7:c.5735A>G	ENSP00000371502.3:p.Gln1912Arg
NM_001079846.1:c.5735A>G	NP_001073315.1:p.Gln1912Arg
NM_004380.2:c.5849A>G	NP_004371.2:p.Gln1950Arg
XM_005255124.3:c.5804A>G	XP_005255181.1:p.Gln1935Arg
XM_005255125.3:c.5432A>G	XP_005255182.1:p.Gln1811Arg
XM_006720848.2:c.5588A>G	XP_006720911.1:p.Gln1863Arg
XM_011522380.1:c.5795A>G	XP_011520682.1:p.Gln1932Arg
XM_011522381.1:c.5096A>G	XP_011520683.1:p.Gln1699Arg
XM_005255124.4:c.5804A>G	XP_005255181.1:p.Gln1935Arg
XM_005255125.4:c.5432A>G	XP_005255182.1:p.Gln1811Arg
XM_006720848.3:c.5588A>G	XP_006720911.1:p.Gln1863Arg
XM_011522381.2:c.5096A>G	XP_011520683.1:p.Gln1699Arg
XM_017022944.1:c.5843A>G	XP_016878433.1:p.Gln1948Arg
NM_004380.3:c.5849A>G MANE Select	NP_004371.2:p.Gln1950Arg