Canonical Allele Identifier: CA493276302
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs2141233848
MyVariant Identifiers: chr16:g.3828108A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3778107A>G , CM000678.2:g.3778107A>G GRCh38
NC_000016.9:g.3828108A>G , CM000678.1:g.3828108A>G GRCh37
NC_000016.8:g.3768109A>G NCBI36
NG_009873.1:g.107014T>C
NG_009873.2:g.107607T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.2017T>C MANE Select ENSP00000262367.5:p.Leu673=
ENST00000262367.9:c.2017T>C ENSP00000262367.5:p.Leu673=
ENST00000382070.7:c.1903T>C ENSP00000371502.3:p.Leu635=
ENST00000570939.2:c.622T>C ENSP00000461002.2:p.Leu208=
ENST00000571826.5:c.66T>C
ENST00000572134.1:c.330T>C
ENST00000634839.1:n.179T>C
NM_001079846.1:c.1903T>C NP_001073315.1:p.Leu635=
NM_004380.2:c.2017T>C NP_004371.2:p.Leu673=
XM_005255124.3:c.2017T>C XP_005255181.1:p.Leu673=
XM_005255125.3:c.2017T>C XP_005255182.1:p.Leu673=
XM_006720848.2:c.2017T>C XP_006720911.1:p.Leu673=
XM_011522380.1:c.1963T>C XP_011520682.1:p.Leu655=
XM_011522381.1:c.1264T>C XP_011520683.1:p.Leu422=
XM_011522382.1:c.2017T>C XP_011520684.1:p.Leu673=
XM_005255124.4:c.2017T>C XP_005255181.1:p.Leu673=
XM_005255125.4:c.2017T>C XP_005255182.1:p.Leu673=
XM_006720848.3:c.2017T>C XP_006720911.1:p.Leu673=
XM_011522381.2:c.1264T>C XP_011520683.1:p.Leu422=
XM_011522382.3:c.2017T>C XP_011520684.1:p.Leu673=
XM_017022944.1:c.2017T>C XP_016878433.1:p.Leu673=
NM_004380.3:c.2017T>C MANE Select NP_004371.2:p.Leu673=