Canonical Allele Identifier: CA394554126
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs2151305935

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3728914G>C , CM000678.2:g.3728914G>C GRCh38
NC_000016.9:g.3778915G>C , CM000678.1:g.3778915G>C GRCh37
NC_000016.8:g.3718916G>C NCBI36
NG_009873.1:g.156207C>G
NG_009873.2:g.156800C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.6133C>G MANE Select ENSP00000262367.5:p.Gln2045Glu
ENST00000262367.9:c.6133C>G ENSP00000262367.5:p.Gln2045Glu
ENST00000382070.7:c.6019C>G ENSP00000371502.3:p.Gln2007Glu
NM_001079846.1:c.6019C>G NP_001073315.1:p.Gln2007Glu
NM_004380.2:c.6133C>G NP_004371.2:p.Gln2045Glu
XM_005255124.3:c.6088C>G XP_005255181.1:p.Gln2030Glu
XM_005255125.3:c.5716C>G XP_005255182.1:p.Gln1906Glu
XM_006720848.2:c.5872C>G XP_006720911.1:p.Gln1958Glu
XM_011522380.1:c.6079C>G XP_011520682.1:p.Gln2027Glu
XM_011522381.1:c.5380C>G XP_011520683.1:p.Gln1794Glu
XM_005255124.4:c.6088C>G XP_005255181.1:p.Gln2030Glu
XM_005255125.4:c.5716C>G XP_005255182.1:p.Gln1906Glu
XM_006720848.3:c.5872C>G XP_006720911.1:p.Gln1958Glu
XM_011522381.2:c.5380C>G XP_011520683.1:p.Gln1794Glu
XM_017022944.1:c.6127C>G XP_016878433.1:p.Gln2043Glu
NM_004380.3:c.6133C>G MANE Select NP_004371.2:p.Gln2045Glu