Canonical Allele Identifier: CA493276274
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs762541030
MyVariant Identifiers: chr16:g.3828058C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3778057C>A , CM000678.2:g.3778057C>A GRCh38
NC_000016.9:g.3828058C>A , CM000678.1:g.3828058C>A GRCh37
NC_000016.8:g.3768059C>A NCBI36
NG_009873.1:g.107064G>T
NG_009873.2:g.107657G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.2067G>T MANE Select ENSP00000262367.5:p.Gly689=
ENST00000262367.9:c.2067G>T ENSP00000262367.5:p.Gly689=
ENST00000382070.7:c.1953G>T ENSP00000371502.3:p.Gly651=
ENST00000570939.2:c.672G>T ENSP00000461002.2:p.Gly224=
ENST00000571826.5:c.116G>T
ENST00000572134.1:c.380G>T
ENST00000634839.1:n.229G>T
NM_001079846.1:c.1953G>T NP_001073315.1:p.Gly651=
NM_004380.2:c.2067G>T NP_004371.2:p.Gly689=
XM_005255124.3:c.2067G>T XP_005255181.1:p.Gly689=
XM_005255125.3:c.2067G>T XP_005255182.1:p.Gly689=
XM_006720848.2:c.2067G>T XP_006720911.1:p.Gly689=
XM_011522380.1:c.2013G>T XP_011520682.1:p.Gly671=
XM_011522381.1:c.1314G>T XP_011520683.1:p.Gly438=
XM_011522382.1:c.2067G>T XP_011520684.1:p.Gly689=
XM_005255124.4:c.2067G>T XP_005255181.1:p.Gly689=
XM_005255125.4:c.2067G>T XP_005255182.1:p.Gly689=
XM_006720848.3:c.2067G>T XP_006720911.1:p.Gly689=
XM_011522381.2:c.1314G>T XP_011520683.1:p.Gly438=
XM_011522382.3:c.2067G>T XP_011520684.1:p.Gly689=
XM_017022944.1:c.2067G>T XP_016878433.1:p.Gly689=
NM_004380.3:c.2067G>T MANE Select NP_004371.2:p.Gly689=