Canonical Allele Identifier: CA394554356

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151306365
• MyVariant Identifiers: chr16:g.3778978C>A (hg19) ; chr16:g.3728977C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728977C>A , CM000678.2:g.3728977C>A	GRCh38
NC_000016.9:g.3778978C>A , CM000678.1:g.3778978C>A	GRCh37
NC_000016.8:g.3718979C>A	NCBI36
NG_009873.1:g.156144G>T
NG_009873.2:g.156737G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6070G>T MANE Select	ENSP00000262367.5:p.Ala2024Ser
ENST00000262367.9:c.6070G>T	ENSP00000262367.5:p.Ala2024Ser
ENST00000382070.7:c.5956G>T	ENSP00000371502.3:p.Ala1986Ser
NM_001079846.1:c.5956G>T	NP_001073315.1:p.Ala1986Ser
NM_004380.2:c.6070G>T	NP_004371.2:p.Ala2024Ser
XM_005255124.3:c.6025G>T	XP_005255181.1:p.Ala2009Ser
XM_005255125.3:c.5653G>T	XP_005255182.1:p.Ala1885Ser
XM_006720848.2:c.5809G>T	XP_006720911.1:p.Ala1937Ser
XM_011522380.1:c.6016G>T	XP_011520682.1:p.Ala2006Ser
XM_011522381.1:c.5317G>T	XP_011520683.1:p.Ala1773Ser
XM_005255124.4:c.6025G>T	XP_005255181.1:p.Ala2009Ser
XM_005255125.4:c.5653G>T	XP_005255182.1:p.Ala1885Ser
XM_006720848.3:c.5809G>T	XP_006720911.1:p.Ala1937Ser
XM_011522381.2:c.5317G>T	XP_011520683.1:p.Ala1773Ser
XM_017022944.1:c.6064G>T	XP_016878433.1:p.Ala2022Ser
NM_004380.3:c.6070G>T MANE Select	NP_004371.2:p.Ala2024Ser