Canonical Allele Identifier: CA2731709264
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs2141232372

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3778003A>C , CM000678.2:g.3778003A>C GRCh38
NC_000016.9:g.3828004A>C , CM000678.1:g.3828004A>C GRCh37
NC_000016.8:g.3768005A>C NCBI36
NG_009873.1:g.107118T>G
NG_009873.2:g.107711T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.2113+8T>G MANE Select ENSP00000262367.5:n.2113+8T>G
ENST00000262367.9:c.2113+8T>G ENSP00000262367.5:n.2113+8T>G
ENST00000382070.7:c.1999+8T>G ENSP00000371502.3:n.1999+8T>G
ENST00000570939.2:c.718+8T>G ENSP00000461002.2:n.718+8T>G
ENST00000571826.5:c.162+8T>G
ENST00000572134.1:c.426+8T>G
ENST00000634839.1:n.283T>G
NM_001079846.1:c.1999+8T>G NP_001073315.1:n.1999+8T>G
NM_004380.2:c.2113+8T>G NP_004371.2:n.2113+8T>G
XM_005255124.3:c.2113+8T>G XP_005255181.1:n.2113+8T>G
XM_005255125.3:c.2113+8T>G XP_005255182.1:n.2113+8T>G
XM_006720848.2:c.2113+8T>G XP_006720911.1:n.2113+8T>G
XM_011522380.1:c.2059+8T>G XP_011520682.1:n.2059+8T>G
XM_011522381.1:c.1360+8T>G XP_011520683.1:n.1360+8T>G
XM_011522382.1:c.2113+8T>G XP_011520684.1:n.2113+8T>G
XM_005255124.4:c.2113+8T>G XP_005255181.1:n.2113+8T>G
XM_005255125.4:c.2113+8T>G XP_005255182.1:n.2113+8T>G
XM_006720848.3:c.2113+8T>G XP_006720911.1:n.2113+8T>G
XM_011522381.2:c.1360+8T>G XP_011520683.1:n.1360+8T>G
XM_011522382.3:c.2113+8T>G XP_011520684.1:n.2113+8T>G
XM_017022944.1:c.2113+8T>G XP_016878433.1:n.2113+8T>G
NM_004380.3:c.2113+8T>G MANE Select NP_004371.2:n.2113+8T>G