Canonical Allele Identifier: CA394554187

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151306047
• gnomAD v4: 16-3728931-A-G
• MyVariant Identifiers: chr16:g.3778932A>G (hg19) ; chr16:g.3728931A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728931A>G , CM000678.2:g.3728931A>G	GRCh38
NC_000016.9:g.3778932A>G , CM000678.1:g.3778932A>G	GRCh37
NC_000016.8:g.3718933A>G	NCBI36
NG_009873.1:g.156190T>C
NG_009873.2:g.156783T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6116T>C MANE Select	ENSP00000262367.5:p.Val2039Ala
ENST00000262367.9:c.6116T>C	ENSP00000262367.5:p.Val2039Ala
ENST00000382070.7:c.6002T>C	ENSP00000371502.3:p.Val2001Ala
NM_001079846.1:c.6002T>C	NP_001073315.1:p.Val2001Ala
NM_004380.2:c.6116T>C	NP_004371.2:p.Val2039Ala
XM_005255124.3:c.6071T>C	XP_005255181.1:p.Val2024Ala
XM_005255125.3:c.5699T>C	XP_005255182.1:p.Val1900Ala
XM_006720848.2:c.5855T>C	XP_006720911.1:p.Val1952Ala
XM_011522380.1:c.6062T>C	XP_011520682.1:p.Val2021Ala
XM_011522381.1:c.5363T>C	XP_011520683.1:p.Val1788Ala
XM_005255124.4:c.6071T>C	XP_005255181.1:p.Val2024Ala
XM_005255125.4:c.5699T>C	XP_005255182.1:p.Val1900Ala
XM_006720848.3:c.5855T>C	XP_006720911.1:p.Val1952Ala
XM_011522381.2:c.5363T>C	XP_011520683.1:p.Val1788Ala
XM_017022944.1:c.6110T>C	XP_016878433.1:p.Val2037Ala
NM_004380.3:c.6116T>C MANE Select	NP_004371.2:p.Val2039Ala