Canonical Allele Identifier: CA973906974
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs1813451264
gnomAD v3: 16-3736855-T-C
gnomAD v4: 16-3736855-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3736855T>C , CM000678.2:g.3736855T>C GRCh38
NC_000016.9:g.3786856T>C , CM000678.1:g.3786856T>C GRCh37
NC_000016.8:g.3726857T>C NCBI36
NG_009873.1:g.148266A>G
NG_009873.2:g.148859A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.4395-40A>G MANE Select ENSP00000262367.5:n.4395-40A>G
ENST00000262367.9:c.4395-40A>G ENSP00000262367.5:n.4395-40A>G
ENST00000382070.7:c.4281-40A>G ENSP00000371502.3:n.4281-40A>G
ENST00000570939.2:c.3030-40A>G ENSP00000461002.2:n.3030-40A>G
ENST00000571763.5:n.145A>G
ENST00000574740.1:n.216-40A>G
ENST00000576720.1:n.3218-40A>G
NM_001079846.1:c.4281-40A>G NP_001073315.1:n.4281-40A>G
NM_004380.2:c.4395-40A>G NP_004371.2:n.4395-40A>G
XM_005255124.3:c.4350-40A>G XP_005255181.1:n.4350-40A>G
XM_005255125.3:c.3978-40A>G XP_005255182.1:n.3978-40A>G
XM_006720848.2:c.4134-40A>G XP_006720911.1:n.4134-40A>G
XM_011522380.1:c.4341-40A>G XP_011520682.1:n.4341-40A>G
XM_011522381.1:c.3642-40A>G XP_011520683.1:n.3642-40A>G
XM_005255124.4:c.4350-40A>G XP_005255181.1:n.4350-40A>G
XM_005255125.4:c.3978-40A>G XP_005255182.1:n.3978-40A>G
XM_006720848.3:c.4134-40A>G XP_006720911.1:n.4134-40A>G
XM_011522381.2:c.3642-40A>G XP_011520683.1:n.3642-40A>G
XM_017022944.1:c.4389-40A>G XP_016878433.1:n.4389-40A>G
NM_004380.3:c.4395-40A>G MANE Select NP_004371.2:n.4395-40A>G