Canonical Allele Identifier: CA394556510

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151311021
• MyVariant Identifiers: chr16:g.3779637T>A (hg19) ; chr16:g.3729636T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729636T>A , CM000678.2:g.3729636T>A	GRCh38
NC_000016.9:g.3779637T>A , CM000678.1:g.3779637T>A	GRCh37
NC_000016.8:g.3719638T>A	NCBI36
NG_009873.1:g.155485A>T
NG_009873.2:g.156078A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5411A>T MANE Select	ENSP00000262367.5:p.His1804Leu
ENST00000262367.9:c.5411A>T	ENSP00000262367.5:p.His1804Leu
ENST00000382070.7:c.5297A>T	ENSP00000371502.3:p.His1766Leu
NM_001079846.1:c.5297A>T	NP_001073315.1:p.His1766Leu
NM_004380.2:c.5411A>T	NP_004371.2:p.His1804Leu
XM_005255124.3:c.5366A>T	XP_005255181.1:p.His1789Leu
XM_005255125.3:c.4994A>T	XP_005255182.1:p.His1665Leu
XM_006720848.2:c.5150A>T	XP_006720911.1:p.His1717Leu
XM_011522380.1:c.5357A>T	XP_011520682.1:p.His1786Leu
XM_011522381.1:c.4658A>T	XP_011520683.1:p.His1553Leu
XM_005255124.4:c.5366A>T	XP_005255181.1:p.His1789Leu
XM_005255125.4:c.4994A>T	XP_005255182.1:p.His1665Leu
XM_006720848.3:c.5150A>T	XP_006720911.1:p.His1717Leu
XM_011522381.2:c.4658A>T	XP_011520683.1:p.His1553Leu
XM_017022944.1:c.5405A>T	XP_016878433.1:p.His1802Leu
NM_004380.3:c.5411A>T MANE Select	NP_004371.2:p.His1804Leu