Canonical Allele Identifier: CA394550103
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs2151297899

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3727740T>C , CM000678.2:g.3727740T>C GRCh38
NC_000016.9:g.3777741T>C , CM000678.1:g.3777741T>C GRCh37
NC_000016.8:g.3717742T>C NCBI36
NG_009873.1:g.157381A>G
NG_009873.2:g.157974A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.7307A>G MANE Select ENSP00000262367.5:p.Glu2436Gly
ENST00000262367.9:c.7307A>G ENSP00000262367.5:p.Glu2436Gly
ENST00000382070.7:c.7193A>G ENSP00000371502.3:p.Glu2398Gly
NM_001079846.1:c.7193A>G NP_001073315.1:p.Glu2398Gly
NM_004380.2:c.7307A>G NP_004371.2:p.Glu2436Gly
XM_005255124.3:c.7262A>G XP_005255181.1:p.Glu2421Gly
XM_005255125.3:c.6890A>G XP_005255182.1:p.Glu2297Gly
XM_006720848.2:c.7046A>G XP_006720911.1:p.Glu2349Gly
XM_011522380.1:c.7253A>G XP_011520682.1:p.Glu2418Gly
XM_011522381.1:c.6554A>G XP_011520683.1:p.Glu2185Gly
XM_005255124.4:c.7262A>G XP_005255181.1:p.Glu2421Gly
XM_005255125.4:c.6890A>G XP_005255182.1:p.Glu2297Gly
XM_006720848.3:c.7046A>G XP_006720911.1:p.Glu2349Gly
XM_011522381.2:c.6554A>G XP_011520683.1:p.Glu2185Gly
XM_017022944.1:c.7301A>G XP_016878433.1:p.Glu2434Gly
NM_004380.3:c.7307A>G MANE Select NP_004371.2:p.Glu2436Gly