Canonical Allele Identifier: CA394550995

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151300086
• gnomAD v4: 16-3728074-G-A
• MyVariant Identifiers: chr16:g.3778075G>A (hg19) ; chr16:g.3728074G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728074G>A , CM000678.2:g.3728074G>A	GRCh38
NC_000016.9:g.3778075G>A , CM000678.1:g.3778075G>A	GRCh37
NC_000016.8:g.3718076G>A	NCBI36
NG_009873.1:g.157047C>T
NG_009873.2:g.157640C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6973C>T MANE Select	ENSP00000262367.5:p.Pro2325Ser
ENST00000262367.9:c.6973C>T	ENSP00000262367.5:p.Pro2325Ser
ENST00000382070.7:c.6859C>T	ENSP00000371502.3:p.Pro2287Ser
NM_001079846.1:c.6859C>T	NP_001073315.1:p.Pro2287Ser
NM_004380.2:c.6973C>T	NP_004371.2:p.Pro2325Ser
XM_005255124.3:c.6928C>T	XP_005255181.1:p.Pro2310Ser
XM_005255125.3:c.6556C>T	XP_005255182.1:p.Pro2186Ser
XM_006720848.2:c.6712C>T	XP_006720911.1:p.Pro2238Ser
XM_011522380.1:c.6919C>T	XP_011520682.1:p.Pro2307Ser
XM_011522381.1:c.6220C>T	XP_011520683.1:p.Pro2074Ser
XM_005255124.4:c.6928C>T	XP_005255181.1:p.Pro2310Ser
XM_005255125.4:c.6556C>T	XP_005255182.1:p.Pro2186Ser
XM_006720848.3:c.6712C>T	XP_006720911.1:p.Pro2238Ser
XM_011522381.2:c.6220C>T	XP_011520683.1:p.Pro2074Ser
XM_017022944.1:c.6967C>T	XP_016878433.1:p.Pro2323Ser
NM_004380.3:c.6973C>T MANE Select	NP_004371.2:p.Pro2325Ser