Canonical Allele Identifier: CA394551018
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs968610522

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3728080C>A , CM000678.2:g.3728080C>A GRCh38
NC_000016.9:g.3778081C>A , CM000678.1:g.3778081C>A GRCh37
NC_000016.8:g.3718082C>A NCBI36
NG_009873.1:g.157041G>T
NG_009873.2:g.157634G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.6967G>T MANE Select ENSP00000262367.5:p.Gly2323Ter
ENST00000262367.9:c.6967G>T ENSP00000262367.5:p.Gly2323Ter
ENST00000382070.7:c.6853G>T ENSP00000371502.3:p.Gly2285Ter
NM_001079846.1:c.6853G>T NP_001073315.1:p.Gly2285Ter
NM_004380.2:c.6967G>T NP_004371.2:p.Gly2323Ter
XM_005255124.3:c.6922G>T XP_005255181.1:p.Gly2308Ter
XM_005255125.3:c.6550G>T XP_005255182.1:p.Gly2184Ter
XM_006720848.2:c.6706G>T XP_006720911.1:p.Gly2236Ter
XM_011522380.1:c.6913G>T XP_011520682.1:p.Gly2305Ter
XM_011522381.1:c.6214G>T XP_011520683.1:p.Gly2072Ter
XM_005255124.4:c.6922G>T XP_005255181.1:p.Gly2308Ter
XM_005255125.4:c.6550G>T XP_005255182.1:p.Gly2184Ter
XM_006720848.3:c.6706G>T XP_006720911.1:p.Gly2236Ter
XM_011522381.2:c.6214G>T XP_011520683.1:p.Gly2072Ter
XM_017022944.1:c.6961G>T XP_016878433.1:p.Gly2321Ter
NM_004380.3:c.6967G>T MANE Select NP_004371.2:p.Gly2323Ter