Canonical Allele Identifier: CA7869313
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs751537328

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3729855T>G , CM000678.2:g.3729855T>G GRCh38
NC_000016.9:g.3779856T>G , CM000678.1:g.3779856T>G GRCh37
NC_000016.8:g.3719857T>G NCBI36
NG_009873.1:g.155266A>C
NG_009873.2:g.155859A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.5192A>C MANE Select ENSP00000262367.5:p.Asn1731Thr
ENST00000262367.9:c.5192A>C ENSP00000262367.5:p.Asn1731Thr
ENST00000382070.7:c.5078A>C ENSP00000371502.3:p.Asn1693Thr
NM_001079846.1:c.5078A>C NP_001073315.1:p.Asn1693Thr
NM_004380.2:c.5192A>C NP_004371.2:p.Asn1731Thr
XM_005255124.3:c.5147A>C XP_005255181.1:p.Asn1716Thr
XM_005255125.3:c.4775A>C XP_005255182.1:p.Asn1592Thr
XM_006720848.2:c.4931A>C XP_006720911.1:p.Asn1644Thr
XM_011522380.1:c.5138A>C XP_011520682.1:p.Asn1713Thr
XM_011522381.1:c.4439A>C XP_011520683.1:p.Asn1480Thr
XM_005255124.4:c.5147A>C XP_005255181.1:p.Asn1716Thr
XM_005255125.4:c.4775A>C XP_005255182.1:p.Asn1592Thr
XM_006720848.3:c.4931A>C XP_006720911.1:p.Asn1644Thr
XM_011522381.2:c.4439A>C XP_011520683.1:p.Asn1480Thr
XM_017022944.1:c.5186A>C XP_016878433.1:p.Asn1729Thr
NM_004380.3:c.5192A>C MANE Select NP_004371.2:p.Asn1731Thr