Canonical Allele Identifier: CA2202971893
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs2053924395
gnomAD v4: 16-3810793-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3810793G>A , CM000678.2:g.3810793G>A GRCh38
NC_000016.9:g.3860794G>A , CM000678.1:g.3860794G>A GRCh37
NC_000016.8:g.3800795G>A NCBI36
NG_009873.1:g.74328C>T
NG_009873.2:g.74921C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.799-14C>T MANE Select ENSP00000262367.5:n.799-14C>T
ENST00000635899.1:n.41-14C>T
ENST00000262367.9:c.799-14C>T ENSP00000262367.5:n.799-14C>T
ENST00000382070.7:c.799-14C>T ENSP00000371502.3:n.799-14C>T
NM_001079846.1:c.799-14C>T NP_001073315.1:n.799-14C>T
NM_004380.2:c.799-14C>T NP_004371.2:n.799-14C>T
XM_005255124.3:c.799-14C>T XP_005255181.1:n.799-14C>T
XM_005255125.3:c.799-14C>T XP_005255182.1:n.799-14C>T
XM_006720848.2:c.799-14C>T XP_006720911.1:n.799-14C>T
XM_011522380.1:c.745-14C>T XP_011520682.1:n.745-14C>T
XM_011522381.1:c.46-14C>T XP_011520683.1:n.46-14C>T
XM_011522382.1:c.799-14C>T XP_011520684.1:n.799-14C>T
XM_005255124.4:c.799-14C>T XP_005255181.1:n.799-14C>T
XM_005255125.4:c.799-14C>T XP_005255182.1:n.799-14C>T
XM_006720848.3:c.799-14C>T XP_006720911.1:n.799-14C>T
XM_011522381.2:c.46-14C>T XP_011520683.1:n.46-14C>T
XM_011522382.3:c.799-14C>T XP_011520684.1:n.799-14C>T
XM_017022944.1:c.799-14C>T XP_016878433.1:n.799-14C>T
NM_004380.3:c.799-14C>T MANE Select NP_004371.2:n.799-14C>T