Canonical Allele Identifier: CA394556039
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs1596787362

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3729498A>T , CM000678.2:g.3729498A>T GRCh38
NC_000016.9:g.3779499A>T , CM000678.1:g.3779499A>T GRCh37
NC_000016.8:g.3719500A>T NCBI36
NG_009873.1:g.155623T>A
NG_009873.2:g.156216T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.5549T>A MANE Select ENSP00000262367.5:p.Leu1850His
ENST00000262367.9:c.5549T>A ENSP00000262367.5:p.Leu1850His
ENST00000382070.7:c.5435T>A ENSP00000371502.3:p.Leu1812His
NM_001079846.1:c.5435T>A NP_001073315.1:p.Leu1812His
NM_004380.2:c.5549T>A NP_004371.2:p.Leu1850His
XM_005255124.3:c.5504T>A XP_005255181.1:p.Leu1835His
XM_005255125.3:c.5132T>A XP_005255182.1:p.Leu1711His
XM_006720848.2:c.5288T>A XP_006720911.1:p.Leu1763His
XM_011522380.1:c.5495T>A XP_011520682.1:p.Leu1832His
XM_011522381.1:c.4796T>A XP_011520683.1:p.Leu1599His
XM_005255124.4:c.5504T>A XP_005255181.1:p.Leu1835His
XM_005255125.4:c.5132T>A XP_005255182.1:p.Leu1711His
XM_006720848.3:c.5288T>A XP_006720911.1:p.Leu1763His
XM_011522381.2:c.4796T>A XP_011520683.1:p.Leu1599His
XM_017022944.1:c.5543T>A XP_016878433.1:p.Leu1848His
NM_004380.3:c.5549T>A MANE Select NP_004371.2:p.Leu1850His