Canonical Allele Identifier: CA394554316

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151306291
• gnomAD v4: 16-3728967-G-T
• MyVariant Identifiers: chr16:g.3778968G>T (hg19) ; chr16:g.3728967G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728967G>T , CM000678.2:g.3728967G>T	GRCh38
NC_000016.9:g.3778968G>T , CM000678.1:g.3778968G>T	GRCh37
NC_000016.8:g.3718969G>T	NCBI36
NG_009873.1:g.156154C>A
NG_009873.2:g.156747C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6080C>A MANE Select	ENSP00000262367.5:p.Pro2027His
ENST00000262367.9:c.6080C>A	ENSP00000262367.5:p.Pro2027His
ENST00000382070.7:c.5966C>A	ENSP00000371502.3:p.Pro1989His
NM_001079846.1:c.5966C>A	NP_001073315.1:p.Pro1989His
NM_004380.2:c.6080C>A	NP_004371.2:p.Pro2027His
XM_005255124.3:c.6035C>A	XP_005255181.1:p.Pro2012His
XM_005255125.3:c.5663C>A	XP_005255182.1:p.Pro1888His
XM_006720848.2:c.5819C>A	XP_006720911.1:p.Pro1940His
XM_011522380.1:c.6026C>A	XP_011520682.1:p.Pro2009His
XM_011522381.1:c.5327C>A	XP_011520683.1:p.Pro1776His
XM_005255124.4:c.6035C>A	XP_005255181.1:p.Pro2012His
XM_005255125.4:c.5663C>A	XP_005255182.1:p.Pro1888His
XM_006720848.3:c.5819C>A	XP_006720911.1:p.Pro1940His
XM_011522381.2:c.5327C>A	XP_011520683.1:p.Pro1776His
XM_017022944.1:c.6074C>A	XP_016878433.1:p.Pro2025His
NM_004380.3:c.6080C>A MANE Select	NP_004371.2:p.Pro2027His