Canonical Allele Identifier: CA394553707

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151304918
• MyVariant Identifiers: chr16:g.3778756C>G (hg19) ; chr16:g.3728755C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728755C>G , CM000678.2:g.3728755C>G	GRCh38
NC_000016.9:g.3778756C>G , CM000678.1:g.3778756C>G	GRCh37
NC_000016.8:g.3718757C>G	NCBI36
NG_009873.1:g.156366G>C
NG_009873.2:g.156959G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6292G>C MANE Select	ENSP00000262367.5:p.Ala2098Pro
ENST00000262367.9:c.6292G>C	ENSP00000262367.5:p.Ala2098Pro
ENST00000382070.7:c.6178G>C	ENSP00000371502.3:p.Ala2060Pro
NM_001079846.1:c.6178G>C	NP_001073315.1:p.Ala2060Pro
NM_004380.2:c.6292G>C	NP_004371.2:p.Ala2098Pro
XM_005255124.3:c.6247G>C	XP_005255181.1:p.Ala2083Pro
XM_005255125.3:c.5875G>C	XP_005255182.1:p.Ala1959Pro
XM_006720848.2:c.6031G>C	XP_006720911.1:p.Ala2011Pro
XM_011522380.1:c.6238G>C	XP_011520682.1:p.Ala2080Pro
XM_011522381.1:c.5539G>C	XP_011520683.1:p.Ala1847Pro
XM_005255124.4:c.6247G>C	XP_005255181.1:p.Ala2083Pro
XM_005255125.4:c.5875G>C	XP_005255182.1:p.Ala1959Pro
XM_006720848.3:c.6031G>C	XP_006720911.1:p.Ala2011Pro
XM_011522381.2:c.5539G>C	XP_011520683.1:p.Ala1847Pro
XM_017022944.1:c.6286G>C	XP_016878433.1:p.Ala2096Pro
NM_004380.3:c.6292G>C MANE Select	NP_004371.2:p.Ala2098Pro