Canonical Allele Identifier: CA394554354

Gene: CREBBP

Linked Data

• dbSNP Id: rs745551441
• gnomAD v4: 16-3728976-G-T
• MyVariant Identifiers: chr16:g.3778977G>T (hg19) ; chr16:g.3728976G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728976G>T , CM000678.2:g.3728976G>T	GRCh38
NC_000016.9:g.3778977G>T , CM000678.1:g.3778977G>T	GRCh37
NC_000016.8:g.3718978G>T	NCBI36
NG_009873.1:g.156145C>A
NG_009873.2:g.156738C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6071C>A MANE Select	ENSP00000262367.5:p.Ala2024Glu
ENST00000262367.9:c.6071C>A	ENSP00000262367.5:p.Ala2024Glu
ENST00000382070.7:c.5957C>A	ENSP00000371502.3:p.Ala1986Glu
NM_001079846.1:c.5957C>A	NP_001073315.1:p.Ala1986Glu
NM_004380.2:c.6071C>A	NP_004371.2:p.Ala2024Glu
XM_005255124.3:c.6026C>A	XP_005255181.1:p.Ala2009Glu
XM_005255125.3:c.5654C>A	XP_005255182.1:p.Ala1885Glu
XM_006720848.2:c.5810C>A	XP_006720911.1:p.Ala1937Glu
XM_011522380.1:c.6017C>A	XP_011520682.1:p.Ala2006Glu
XM_011522381.1:c.5318C>A	XP_011520683.1:p.Ala1773Glu
XM_005255124.4:c.6026C>A	XP_005255181.1:p.Ala2009Glu
XM_005255125.4:c.5654C>A	XP_005255182.1:p.Ala1885Glu
XM_006720848.3:c.5810C>A	XP_006720911.1:p.Ala1937Glu
XM_011522381.2:c.5318C>A	XP_011520683.1:p.Ala1773Glu
XM_017022944.1:c.6065C>A	XP_016878433.1:p.Ala2022Glu
NM_004380.3:c.6071C>A MANE Select	NP_004371.2:p.Ala2024Glu