Canonical Allele Identifier: CA394550384

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151298802
• MyVariant Identifiers: chr16:g.3777875C>G (hg19) ; chr16:g.3727874C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3727874C>G , CM000678.2:g.3727874C>G	GRCh38
NC_000016.9:g.3777875C>G , CM000678.1:g.3777875C>G	GRCh37
NC_000016.8:g.3717876C>G	NCBI36
NG_009873.1:g.157247G>C
NG_009873.2:g.157840G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.7173G>C MANE Select	ENSP00000262367.5:p.Met2391Ile
ENST00000262367.9:c.7173G>C	ENSP00000262367.5:p.Met2391Ile
ENST00000382070.7:c.7059G>C	ENSP00000371502.3:p.Met2353Ile
NM_001079846.1:c.7059G>C	NP_001073315.1:p.Met2353Ile
NM_004380.2:c.7173G>C	NP_004371.2:p.Met2391Ile
XM_005255124.3:c.7128G>C	XP_005255181.1:p.Met2376Ile
XM_005255125.3:c.6756G>C	XP_005255182.1:p.Met2252Ile
XM_006720848.2:c.6912G>C	XP_006720911.1:p.Met2304Ile
XM_011522380.1:c.7119G>C	XP_011520682.1:p.Met2373Ile
XM_011522381.1:c.6420G>C	XP_011520683.1:p.Met2140Ile
XM_005255124.4:c.7128G>C	XP_005255181.1:p.Met2376Ile
XM_005255125.4:c.6756G>C	XP_005255182.1:p.Met2252Ile
XM_006720848.3:c.6912G>C	XP_006720911.1:p.Met2304Ile
XM_011522381.2:c.6420G>C	XP_011520683.1:p.Met2140Ile
XM_017022944.1:c.7167G>C	XP_016878433.1:p.Met2389Ile
NM_004380.3:c.7173G>C MANE Select	NP_004371.2:p.Met2391Ile