Canonical Allele Identifier: CA394557819

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151312741
• gnomAD v4: 16-3729868-C-T
• MyVariant Identifiers: chr16:g.3779869C>T (hg19) ; chr16:g.3729868C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729868C>T , CM000678.2:g.3729868C>T	GRCh38
NC_000016.9:g.3779869C>T , CM000678.1:g.3779869C>T	GRCh37
NC_000016.8:g.3719870C>T	NCBI36
NG_009873.1:g.155253G>A
NG_009873.2:g.155846G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5179G>A MANE Select	ENSP00000262367.5:p.Asp1727Asn
ENST00000262367.9:c.5179G>A	ENSP00000262367.5:p.Asp1727Asn
ENST00000382070.7:c.5065G>A	ENSP00000371502.3:p.Asp1689Asn
NM_001079846.1:c.5065G>A	NP_001073315.1:p.Asp1689Asn
NM_004380.2:c.5179G>A	NP_004371.2:p.Asp1727Asn
XM_005255124.3:c.5134G>A	XP_005255181.1:p.Asp1712Asn
XM_005255125.3:c.4762G>A	XP_005255182.1:p.Asp1588Asn
XM_006720848.2:c.4918G>A	XP_006720911.1:p.Asp1640Asn
XM_011522380.1:c.5125G>A	XP_011520682.1:p.Asp1709Asn
XM_011522381.1:c.4426G>A	XP_011520683.1:p.Asp1476Asn
XM_005255124.4:c.5134G>A	XP_005255181.1:p.Asp1712Asn
XM_005255125.4:c.4762G>A	XP_005255182.1:p.Asp1588Asn
XM_006720848.3:c.4918G>A	XP_006720911.1:p.Asp1640Asn
XM_011522381.2:c.4426G>A	XP_011520683.1:p.Asp1476Asn
XM_017022944.1:c.5173G>A	XP_016878433.1:p.Asp1725Asn
NM_004380.3:c.5179G>A MANE Select	NP_004371.2:p.Asp1727Asn