Canonical Allele Identifier: CA394554212

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151306131
• MyVariant Identifiers: chr16:g.3778943C>G (hg19) ; chr16:g.3728942C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728942C>G , CM000678.2:g.3728942C>G	GRCh38
NC_000016.9:g.3778943C>G , CM000678.1:g.3778943C>G	GRCh37
NC_000016.8:g.3718944C>G	NCBI36
NG_009873.1:g.156179G>C
NG_009873.2:g.156772G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000262367.10:c.6105G>C MANE Select	ENSP00000262367.5:p.Leu2035Phe
ENST00000262367.9:c.6105G>C	ENSP00000262367.5:p.Leu2035Phe
ENST00000382070.7:c.5991G>C	ENSP00000371502.3:p.Leu1997Phe
NM_001079846.1:c.5991G>C	NP_001073315.1:p.Leu1997Phe
NM_004380.2:c.6105G>C	NP_004371.2:p.Leu2035Phe
XM_005255124.3:c.6060G>C	XP_005255181.1:p.Leu2020Phe
XM_005255125.3:c.5688G>C	XP_005255182.1:p.Leu1896Phe
XM_006720848.2:c.5844G>C	XP_006720911.1:p.Leu1948Phe
XM_011522380.1:c.6051G>C	XP_011520682.1:p.Leu2017Phe
XM_011522381.1:c.5352G>C	XP_011520683.1:p.Leu1784Phe
XM_005255124.4:c.6060G>C	XP_005255181.1:p.Leu2020Phe
XM_005255125.4:c.5688G>C	XP_005255182.1:p.Leu1896Phe
XM_006720848.3:c.5844G>C	XP_006720911.1:p.Leu1948Phe
XM_011522381.2:c.5352G>C	XP_011520683.1:p.Leu1784Phe
XM_017022944.1:c.6099G>C	XP_016878433.1:p.Leu2033Phe
NM_004380.3:c.6105G>C MANE Select	NP_004371.2:p.Leu2035Phe