Canonical Allele Identifier: CA394550446

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151298999
• gnomAD v4: 16-3727905-C-G
• MyVariant Identifiers: chr16:g.3777906C>G (hg19) ; chr16:g.3727905C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3727905C>G , CM000678.2:g.3727905C>G	GRCh38
NC_000016.9:g.3777906C>G , CM000678.1:g.3777906C>G	GRCh37
NC_000016.8:g.3717907C>G	NCBI36
NG_009873.1:g.157216G>C
NG_009873.2:g.157809G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.7142G>C MANE Select	ENSP00000262367.5:p.Gly2381Ala
ENST00000262367.9:c.7142G>C	ENSP00000262367.5:p.Gly2381Ala
ENST00000382070.7:c.7028G>C	ENSP00000371502.3:p.Gly2343Ala
NM_001079846.1:c.7028G>C	NP_001073315.1:p.Gly2343Ala
NM_004380.2:c.7142G>C	NP_004371.2:p.Gly2381Ala
XM_005255124.3:c.7097G>C	XP_005255181.1:p.Gly2366Ala
XM_005255125.3:c.6725G>C	XP_005255182.1:p.Gly2242Ala
XM_006720848.2:c.6881G>C	XP_006720911.1:p.Gly2294Ala
XM_011522380.1:c.7088G>C	XP_011520682.1:p.Gly2363Ala
XM_011522381.1:c.6389G>C	XP_011520683.1:p.Gly2130Ala
XM_005255124.4:c.7097G>C	XP_005255181.1:p.Gly2366Ala
XM_005255125.4:c.6725G>C	XP_005255182.1:p.Gly2242Ala
XM_006720848.3:c.6881G>C	XP_006720911.1:p.Gly2294Ala
XM_011522381.2:c.6389G>C	XP_011520683.1:p.Gly2130Ala
XM_017022944.1:c.7136G>C	XP_016878433.1:p.Gly2379Ala
NM_004380.3:c.7142G>C MANE Select	NP_004371.2:p.Gly2381Ala