Canonical Allele Identifier: CA493393663

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151305075
• MyVariant Identifiers: chr16:g.3778784G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728783G>A , CM000678.2:g.3728783G>A	GRCh38
NC_000016.9:g.3778784G>A , CM000678.1:g.3778784G>A	GRCh37
NC_000016.8:g.3718785G>A	NCBI36
NG_009873.1:g.156338C>T
NG_009873.2:g.156931C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6264C>T MANE Select	ENSP00000262367.5:p.Asn2088=
ENST00000262367.9:c.6264C>T	ENSP00000262367.5:p.Asn2088=
ENST00000382070.7:c.6150C>T	ENSP00000371502.3:p.Asn2050=
NM_001079846.1:c.6150C>T	NP_001073315.1:p.Asn2050=
NM_004380.2:c.6264C>T	NP_004371.2:p.Asn2088=
XM_005255124.3:c.6219C>T	XP_005255181.1:p.Asn2073=
XM_005255125.3:c.5847C>T	XP_005255182.1:p.Asn1949=
XM_006720848.2:c.6003C>T	XP_006720911.1:p.Asn2001=
XM_011522380.1:c.6210C>T	XP_011520682.1:p.Asn2070=
XM_011522381.1:c.5511C>T	XP_011520683.1:p.Asn1837=
XM_005255124.4:c.6219C>T	XP_005255181.1:p.Asn2073=
XM_005255125.4:c.5847C>T	XP_005255182.1:p.Asn1949=
XM_006720848.3:c.6003C>T	XP_006720911.1:p.Asn2001=
XM_011522381.2:c.5511C>T	XP_011520683.1:p.Asn1837=
XM_017022944.1:c.6258C>T	XP_016878433.1:p.Asn2086=
NM_004380.3:c.6264C>T MANE Select	NP_004371.2:p.Asn2088=