Canonical Allele Identifier: CA394554520

Gene: CREBBP

Linked Data

• dbSNP Id: rs1451288396
• gnomAD v4: 16-3729015-G-C
• MyVariant Identifiers: chr16:g.3779016G>C (hg19) ; chr16:g.3729015G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729015G>C , CM000678.2:g.3729015G>C	GRCh38
NC_000016.9:g.3779016G>C , CM000678.1:g.3779016G>C	GRCh37
NC_000016.8:g.3719017G>C	NCBI36
NG_009873.1:g.156106C>G
NG_009873.2:g.156699C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6032C>G MANE Select	ENSP00000262367.5:p.Pro2011Arg
ENST00000262367.9:c.6032C>G	ENSP00000262367.5:p.Pro2011Arg
ENST00000382070.7:c.5918C>G	ENSP00000371502.3:p.Pro1973Arg
NM_001079846.1:c.5918C>G	NP_001073315.1:p.Pro1973Arg
NM_004380.2:c.6032C>G	NP_004371.2:p.Pro2011Arg
XM_005255124.3:c.5987C>G	XP_005255181.1:p.Pro1996Arg
XM_005255125.3:c.5615C>G	XP_005255182.1:p.Pro1872Arg
XM_006720848.2:c.5771C>G	XP_006720911.1:p.Pro1924Arg
XM_011522380.1:c.5978C>G	XP_011520682.1:p.Pro1993Arg
XM_011522381.1:c.5279C>G	XP_011520683.1:p.Pro1760Arg
XM_005255124.4:c.5987C>G	XP_005255181.1:p.Pro1996Arg
XM_005255125.4:c.5615C>G	XP_005255182.1:p.Pro1872Arg
XM_006720848.3:c.5771C>G	XP_006720911.1:p.Pro1924Arg
XM_011522381.2:c.5279C>G	XP_011520683.1:p.Pro1760Arg
XM_017022944.1:c.6026C>G	XP_016878433.1:p.Pro2009Arg
NM_004380.3:c.6032C>G MANE Select	NP_004371.2:p.Pro2011Arg