Canonical Allele Identifier: CA394563596

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151329497
• MyVariant Identifiers: chr16:g.3786711C>G (hg19) ; chr16:g.3736710C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3736710C>G , CM000678.2:g.3736710C>G	GRCh38
NC_000016.9:g.3786711C>G , CM000678.1:g.3786711C>G	GRCh37
NC_000016.8:g.3726712C>G	NCBI36
NG_009873.1:g.148411G>C
NG_009873.2:g.149004G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.4500G>C MANE Select	ENSP00000262367.5:p.Gln1500His
ENST00000262367.9:c.4500G>C	ENSP00000262367.5:p.Gln1500His
ENST00000382070.7:c.4386G>C	ENSP00000371502.3:p.Gln1462His
ENST00000570939.2:c.3135G>C	ENSP00000461002.2:p.Gln1045His
ENST00000571763.5:n.290G>C
ENST00000574740.1:n.321G>C
ENST00000576720.1:n.3323G>C
NM_001079846.1:c.4386G>C	NP_001073315.1:p.Gln1462His
NM_004380.2:c.4500G>C	NP_004371.2:p.Gln1500His
XM_005255124.3:c.4455G>C	XP_005255181.1:p.Gln1485His
XM_005255125.3:c.4083G>C	XP_005255182.1:p.Gln1361His
XM_006720848.2:c.4239G>C	XP_006720911.1:p.Gln1413His
XM_011522380.1:c.4446G>C	XP_011520682.1:p.Gln1482His
XM_011522381.1:c.3747G>C	XP_011520683.1:p.Gln1249His
XM_005255124.4:c.4455G>C	XP_005255181.1:p.Gln1485His
XM_005255125.4:c.4083G>C	XP_005255182.1:p.Gln1361His
XM_006720848.3:c.4239G>C	XP_006720911.1:p.Gln1413His
XM_011522381.2:c.3747G>C	XP_011520683.1:p.Gln1249His
XM_017022944.1:c.4494G>C	XP_016878433.1:p.Gln1498His
NM_004380.3:c.4500G>C MANE Select	NP_004371.2:p.Gln1500His