Canonical Allele Identifier: CA394553788

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151305132
• MyVariant Identifiers: chr16:g.3778792C>T (hg19) ; chr16:g.3728791C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728791C>T , CM000678.2:g.3728791C>T	GRCh38
NC_000016.9:g.3778792C>T , CM000678.1:g.3778792C>T	GRCh37
NC_000016.8:g.3718793C>T	NCBI36
NG_009873.1:g.156330G>A
NG_009873.2:g.156923G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6256G>A MANE Select	ENSP00000262367.5:p.Val2086Met
ENST00000262367.9:c.6256G>A	ENSP00000262367.5:p.Val2086Met
ENST00000382070.7:c.6142G>A	ENSP00000371502.3:p.Val2048Met
NM_001079846.1:c.6142G>A	NP_001073315.1:p.Val2048Met
NM_004380.2:c.6256G>A	NP_004371.2:p.Val2086Met
XM_005255124.3:c.6211G>A	XP_005255181.1:p.Val2071Met
XM_005255125.3:c.5839G>A	XP_005255182.1:p.Val1947Met
XM_006720848.2:c.5995G>A	XP_006720911.1:p.Val1999Met
XM_011522380.1:c.6202G>A	XP_011520682.1:p.Val2068Met
XM_011522381.1:c.5503G>A	XP_011520683.1:p.Val1835Met
XM_005255124.4:c.6211G>A	XP_005255181.1:p.Val2071Met
XM_005255125.4:c.5839G>A	XP_005255182.1:p.Val1947Met
XM_006720848.3:c.5995G>A	XP_006720911.1:p.Val1999Met
XM_011522381.2:c.5503G>A	XP_011520683.1:p.Val1835Met
XM_017022944.1:c.6250G>A	XP_016878433.1:p.Val2084Met
NM_004380.3:c.6256G>A MANE Select	NP_004371.2:p.Val2086Met