Canonical Allele Identifier: CA394555184

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151307690
• gnomAD v4: 16-3729186-G-A
• MyVariant Identifiers: chr16:g.3779187G>A (hg19) ; chr16:g.3729186G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729186G>A , CM000678.2:g.3729186G>A	GRCh38
NC_000016.9:g.3779187G>A , CM000678.1:g.3779187G>A	GRCh37
NC_000016.8:g.3719188G>A	NCBI36
NG_009873.1:g.155935C>T
NG_009873.2:g.156528C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5861C>T MANE Select	ENSP00000262367.5:p.Ala1954Val
ENST00000262367.9:c.5861C>T	ENSP00000262367.5:p.Ala1954Val
ENST00000382070.7:c.5747C>T	ENSP00000371502.3:p.Ala1916Val
NM_001079846.1:c.5747C>T	NP_001073315.1:p.Ala1916Val
NM_004380.2:c.5861C>T	NP_004371.2:p.Ala1954Val
XM_005255124.3:c.5816C>T	XP_005255181.1:p.Ala1939Val
XM_005255125.3:c.5444C>T	XP_005255182.1:p.Ala1815Val
XM_006720848.2:c.5600C>T	XP_006720911.1:p.Ala1867Val
XM_011522380.1:c.5807C>T	XP_011520682.1:p.Ala1936Val
XM_011522381.1:c.5108C>T	XP_011520683.1:p.Ala1703Val
XM_005255124.4:c.5816C>T	XP_005255181.1:p.Ala1939Val
XM_005255125.4:c.5444C>T	XP_005255182.1:p.Ala1815Val
XM_006720848.3:c.5600C>T	XP_006720911.1:p.Ala1867Val
XM_011522381.2:c.5108C>T	XP_011520683.1:p.Ala1703Val
XM_017022944.1:c.5855C>T	XP_016878433.1:p.Ala1952Val
NM_004380.3:c.5861C>T MANE Select	NP_004371.2:p.Ala1954Val