Canonical Allele Identifier: CA276979757

Gene: CREBBP

Linked Data

• dbSNP Id: rs965021325
• gnomAD v4: 16-3736319-A-C
• MyVariant Identifiers: chr16:g.3786320A>C (hg19) ; chr16:g.3736319A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3736319A>C , CM000678.2:g.3736319A>C	GRCh38
NC_000016.9:g.3786320A>C , CM000678.1:g.3786320A>C	GRCh37
NC_000016.8:g.3726321A>C	NCBI36
NG_009873.1:g.148802T>G
NG_009873.2:g.149395T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.4561-116T>G MANE Select	ENSP00000262367.5:n.4561-116T>G
ENST00000262367.9:c.4561-116T>G	ENSP00000262367.5:n.4561-116T>G
ENST00000382070.7:c.4447-116T>G	ENSP00000371502.3:n.4447-116T>G
ENST00000570939.2:c.3196-116T>G	ENSP00000461002.2:n.3196-116T>G
ENST00000571763.5:n.351-116T>G
ENST00000576720.1:n.3384-116T>G
NM_001079846.1:c.4447-116T>G	NP_001073315.1:n.4447-116T>G
NM_004380.2:c.4561-116T>G	NP_004371.2:n.4561-116T>G
XM_005255124.3:c.4516-116T>G	XP_005255181.1:n.4516-116T>G
XM_005255125.3:c.4144-116T>G	XP_005255182.1:n.4144-116T>G
XM_006720848.2:c.4300-116T>G	XP_006720911.1:n.4300-116T>G
XM_011522380.1:c.4507-116T>G	XP_011520682.1:n.4507-116T>G
XM_011522381.1:c.3808-116T>G	XP_011520683.1:n.3808-116T>G
XM_005255124.4:c.4516-116T>G	XP_005255181.1:n.4516-116T>G
XM_005255125.4:c.4144-116T>G	XP_005255182.1:n.4144-116T>G
XM_006720848.3:c.4300-116T>G	XP_006720911.1:n.4300-116T>G
XM_011522381.2:c.3808-116T>G	XP_011520683.1:n.3808-116T>G
XM_017022944.1:c.4555-116T>G	XP_016878433.1:n.4555-116T>G
NM_004380.3:c.4561-116T>G MANE Select	NP_004371.2:n.4561-116T>G