Canonical Allele Identifier: CA394556056
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs2151310038

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3729504T>A , CM000678.2:g.3729504T>A GRCh38
NC_000016.9:g.3779505T>A , CM000678.1:g.3779505T>A GRCh37
NC_000016.8:g.3719506T>A NCBI36
NG_009873.1:g.155617A>T
NG_009873.2:g.156210A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.5543A>T MANE Select ENSP00000262367.5:p.His1848Leu
ENST00000262367.9:c.5543A>T ENSP00000262367.5:p.His1848Leu
ENST00000382070.7:c.5429A>T ENSP00000371502.3:p.His1810Leu
NM_001079846.1:c.5429A>T NP_001073315.1:p.His1810Leu
NM_004380.2:c.5543A>T NP_004371.2:p.His1848Leu
XM_005255124.3:c.5498A>T XP_005255181.1:p.His1833Leu
XM_005255125.3:c.5126A>T XP_005255182.1:p.His1709Leu
XM_006720848.2:c.5282A>T XP_006720911.1:p.His1761Leu
XM_011522380.1:c.5489A>T XP_011520682.1:p.His1830Leu
XM_011522381.1:c.4790A>T XP_011520683.1:p.His1597Leu
XM_005255124.4:c.5498A>T XP_005255181.1:p.His1833Leu
XM_005255125.4:c.5126A>T XP_005255182.1:p.His1709Leu
XM_006720848.3:c.5282A>T XP_006720911.1:p.His1761Leu
XM_011522381.2:c.4790A>T XP_011520683.1:p.His1597Leu
XM_017022944.1:c.5537A>T XP_016878433.1:p.His1846Leu
NM_004380.3:c.5543A>T MANE Select NP_004371.2:p.His1848Leu