Canonical Allele Identifier: CA394562376
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs2141496479

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3850911C>A , CM000678.2:g.3850911C>A GRCh38
NC_000016.9:g.3900912C>A , CM000678.1:g.3900912C>A GRCh37
NC_000016.8:g.3840913C>A NCBI36
NG_009873.1:g.34210G>T
NG_009873.2:g.34803G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000262367.10:c.184G>T MANE Select ENSP00000262367.5:p.Asp62Tyr
ENST00000262367.9:c.184G>T ENSP00000262367.5:p.Asp62Tyr
ENST00000382070.7:c.184G>T ENSP00000371502.3:p.Asp62Tyr
NM_001079846.1:c.184G>T NP_001073315.1:p.Asp62Tyr
NM_004380.2:c.184G>T NP_004371.2:p.Asp62Tyr
XM_005255124.3:c.184G>T XP_005255181.1:p.Asp62Tyr
XM_005255125.3:c.184G>T XP_005255182.1:p.Asp62Tyr
XM_006720848.2:c.184G>T XP_006720911.1:p.Asp62Tyr
XM_011522380.1:c.130G>T XP_011520682.1:p.Asp44Tyr
XM_011522382.1:c.184G>T XP_011520684.1:p.Asp62Tyr
XM_005255124.4:c.184G>T XP_005255181.1:p.Asp62Tyr
XM_005255125.4:c.184G>T XP_005255182.1:p.Asp62Tyr
XM_006720848.3:c.184G>T XP_006720911.1:p.Asp62Tyr
XM_011522382.3:c.184G>T XP_011520684.1:p.Asp62Tyr
XM_017022944.1:c.184G>T XP_016878433.1:p.Asp62Tyr
NM_004380.3:c.184G>T MANE Select NP_004371.2:p.Asp62Tyr