Canonical Allele Identifier: CA493395107
Gene: CREBBP HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.3820856G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3770855G>C , CM000678.2:g.3770855G>C GRCh38
NC_000016.9:g.3820856G>C , CM000678.1:g.3820856G>C GRCh37
NC_000016.8:g.3760857G>C NCBI36
NG_009873.1:g.114266C>G
NG_009873.2:g.114859C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262367.10:c.2595C>G MANE Select ENSP00000262367.5:p.Gly865=
ENST00000262367.9:c.2595C>G ENSP00000262367.5:p.Gly865=
ENST00000382070.7:c.2481C>G ENSP00000371502.3:p.Gly827=
ENST00000570939.2:c.1200C>G ENSP00000461002.2:p.Gly400=
NM_001079846.1:c.2481C>G NP_001073315.1:p.Gly827=
NM_004380.2:c.2595C>G NP_004371.2:p.Gly865=
XM_005255124.3:c.2550C>G XP_005255181.1:p.Gly850=
XM_005255125.3:c.2464-1502C>G XP_005255182.1:n.2464-1502C>G
XM_006720848.2:c.2595C>G XP_006720911.1:p.Gly865=
XM_011522380.1:c.2541C>G XP_011520682.1:p.Gly847=
XM_011522381.1:c.1842C>G XP_011520683.1:p.Gly614=
XM_011522382.1:c.2595C>G XP_011520684.1:p.Gly865=
XM_005255124.4:c.2550C>G XP_005255181.1:p.Gly850=
XM_005255125.4:c.2464-1502C>G XP_005255182.1:n.2464-1502C>G
XM_006720848.3:c.2595C>G XP_006720911.1:p.Gly865=
XM_011522381.2:c.1842C>G XP_011520683.1:p.Gly614=
XM_011522382.3:c.2595C>G XP_011520684.1:p.Gly865=
XM_017022944.1:c.2589C>G XP_016878433.1:p.Gly863=
NM_004380.3:c.2595C>G MANE Select NP_004371.2:p.Gly865=