Canonical Allele Identifier: CA394559141

Gene: CREBBP

Linked Data

• dbSNP Id: rs1597052973
• MyVariant Identifiers: chr16:g.3900296A>C (hg19) ; chr16:g.3850295A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3850295A>C , CM000678.2:g.3850295A>C	GRCh38
NC_000016.9:g.3900296A>C , CM000678.1:g.3900296A>C	GRCh37
NC_000016.8:g.3840297A>C	NCBI36
NG_009873.1:g.34826T>G
NG_009873.2:g.35419T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.798+2T>G MANE Select	ENSP00000262367.5:n.798+2T>G
ENST00000636895.1:n.25+2T>G
ENST00000262367.9:c.798+2T>G	ENSP00000262367.5:n.798+2T>G
ENST00000382070.7:c.798+2T>G	ENSP00000371502.3:n.798+2T>G
NM_001079846.1:c.798+2T>G	NP_001073315.1:n.798+2T>G
NM_004380.2:c.798+2T>G	NP_004371.2:n.798+2T>G
XM_005255124.3:c.798+2T>G	XP_005255181.1:n.798+2T>G
XM_005255125.3:c.798+2T>G	XP_005255182.1:n.798+2T>G
XM_006720848.2:c.798+2T>G	XP_006720911.1:n.798+2T>G
XM_011522380.1:c.744+2T>G	XP_011520682.1:n.744+2T>G
XM_011522382.1:c.798+2T>G	XP_011520684.1:n.798+2T>G
XM_005255124.4:c.798+2T>G	XP_005255181.1:n.798+2T>G
XM_005255125.4:c.798+2T>G	XP_005255182.1:n.798+2T>G
XM_006720848.3:c.798+2T>G	XP_006720911.1:n.798+2T>G
XM_011522382.3:c.798+2T>G	XP_011520684.1:n.798+2T>G
XM_017022944.1:c.798+2T>G	XP_016878433.1:n.798+2T>G
NM_004380.3:c.798+2T>G MANE Select	NP_004371.2:n.798+2T>G