Canonical Allele Identifier: CA394555989

Gene: CREBBP

Linked Data

• dbSNP Id: rs1204228560
• MyVariant Identifiers: chr16:g.3779476G>C (hg19) ; chr16:g.3729475G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729475G>C , CM000678.2:g.3729475G>C	GRCh38
NC_000016.9:g.3779476G>C , CM000678.1:g.3779476G>C	GRCh37
NC_000016.8:g.3719477G>C	NCBI36
NG_009873.1:g.155646C>G
NG_009873.2:g.156239C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5572C>G MANE Select	ENSP00000262367.5:p.Arg1858Gly
ENST00000262367.9:c.5572C>G	ENSP00000262367.5:p.Arg1858Gly
ENST00000382070.7:c.5458C>G	ENSP00000371502.3:p.Arg1820Gly
NM_001079846.1:c.5458C>G	NP_001073315.1:p.Arg1820Gly
NM_004380.2:c.5572C>G	NP_004371.2:p.Arg1858Gly
XM_005255124.3:c.5527C>G	XP_005255181.1:p.Arg1843Gly
XM_005255125.3:c.5155C>G	XP_005255182.1:p.Arg1719Gly
XM_006720848.2:c.5311C>G	XP_006720911.1:p.Arg1771Gly
XM_011522380.1:c.5518C>G	XP_011520682.1:p.Arg1840Gly
XM_011522381.1:c.4819C>G	XP_011520683.1:p.Arg1607Gly
XM_005255124.4:c.5527C>G	XP_005255181.1:p.Arg1843Gly
XM_005255125.4:c.5155C>G	XP_005255182.1:p.Arg1719Gly
XM_006720848.3:c.5311C>G	XP_006720911.1:p.Arg1771Gly
XM_011522381.2:c.4819C>G	XP_011520683.1:p.Arg1607Gly
XM_017022944.1:c.5566C>G	XP_016878433.1:p.Arg1856Gly
NM_004380.3:c.5572C>G MANE Select	NP_004371.2:p.Arg1858Gly