Canonical Allele Identifier: CA7870271

Gene: CREBBP

Linked Data

• ClinVar Variation Id: 2075598
• ClinVar RCV Id: RCV002967850
• dbSNP Id: rs371905531
• ExAC: 16:3827993 T / C
• gnomAD v2: 16-3827993-T-C
• gnomAD v3: 16-3777992-T-C
• gnomAD v4: 16-3777992-T-C
• MyVariant Identifiers: chr16:g.3827993T>C (hg19) ; chr16:g.3777992T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3777992T>C , CM000678.2:g.3777992T>C	GRCh38
NC_000016.9:g.3827993T>C , CM000678.1:g.3827993T>C	GRCh37
NC_000016.8:g.3767994T>C	NCBI36
NG_009873.1:g.107129A>G
NG_009873.2:g.107722A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.2113+19A>G MANE Select	ENSP00000262367.5:n.2113+19A>G
ENST00000262367.9:c.2113+19A>G	ENSP00000262367.5:n.2113+19A>G
ENST00000382070.7:c.1999+19A>G	ENSP00000371502.3:n.1999+19A>G
ENST00000570939.2:c.718+19A>G	ENSP00000461002.2:n.718+19A>G
ENST00000571826.5:c.162+19A>G
ENST00000572134.1:c.426+19A>G
ENST00000634839.1:n.294A>G
NM_001079846.1:c.1999+19A>G	NP_001073315.1:n.1999+19A>G
NM_004380.2:c.2113+19A>G	NP_004371.2:n.2113+19A>G
XM_005255124.3:c.2113+19A>G	XP_005255181.1:n.2113+19A>G
XM_005255125.3:c.2113+19A>G	XP_005255182.1:n.2113+19A>G
XM_006720848.2:c.2113+19A>G	XP_006720911.1:n.2113+19A>G
XM_011522380.1:c.2059+19A>G	XP_011520682.1:n.2059+19A>G
XM_011522381.1:c.1360+19A>G	XP_011520683.1:n.1360+19A>G
XM_011522382.1:c.2113+19A>G	XP_011520684.1:n.2113+19A>G
XM_005255124.4:c.2113+19A>G	XP_005255181.1:n.2113+19A>G
XM_005255125.4:c.2113+19A>G	XP_005255182.1:n.2113+19A>G
XM_006720848.3:c.2113+19A>G	XP_006720911.1:n.2113+19A>G
XM_011522381.2:c.1360+19A>G	XP_011520683.1:n.1360+19A>G
XM_011522382.3:c.2113+19A>G	XP_011520684.1:n.2113+19A>G
XM_017022944.1:c.2113+19A>G	XP_016878433.1:n.2113+19A>G
NM_004380.3:c.2113+19A>G MANE Select	NP_004371.2:n.2113+19A>G