Canonical Allele Identifier: CA394556439

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151310889
• MyVariant Identifiers: chr16:g.3779619C>G (hg19) ; chr16:g.3729618C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729618C>G , CM000678.2:g.3729618C>G	GRCh38
NC_000016.9:g.3779619C>G , CM000678.1:g.3779619C>G	GRCh37
NC_000016.8:g.3719620C>G	NCBI36
NG_009873.1:g.155503G>C
NG_009873.2:g.156096G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5429G>C MANE Select	ENSP00000262367.5:p.Arg1810Pro
ENST00000262367.9:c.5429G>C	ENSP00000262367.5:p.Arg1810Pro
ENST00000382070.7:c.5315G>C	ENSP00000371502.3:p.Arg1772Pro
NM_001079846.1:c.5315G>C	NP_001073315.1:p.Arg1772Pro
NM_004380.2:c.5429G>C	NP_004371.2:p.Arg1810Pro
XM_005255124.3:c.5384G>C	XP_005255181.1:p.Arg1795Pro
XM_005255125.3:c.5012G>C	XP_005255182.1:p.Arg1671Pro
XM_006720848.2:c.5168G>C	XP_006720911.1:p.Arg1723Pro
XM_011522380.1:c.5375G>C	XP_011520682.1:p.Arg1792Pro
XM_011522381.1:c.4676G>C	XP_011520683.1:p.Arg1559Pro
XM_005255124.4:c.5384G>C	XP_005255181.1:p.Arg1795Pro
XM_005255125.4:c.5012G>C	XP_005255182.1:p.Arg1671Pro
XM_006720848.3:c.5168G>C	XP_006720911.1:p.Arg1723Pro
XM_011522381.2:c.4676G>C	XP_011520683.1:p.Arg1559Pro
XM_017022944.1:c.5423G>C	XP_016878433.1:p.Arg1808Pro
NM_004380.3:c.5429G>C MANE Select	NP_004371.2:p.Arg1810Pro