Canonical Allele Identifier: CA276979773
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs540370049
MyVariant Identifiers: chr16:g.3736328C>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3736328C>G , CM000678.2:g.3736328C>G GRCh38
NC_000016.9:g.3786329C>G , CM000678.1:g.3786329C>G GRCh37
NC_000016.8:g.3726330C>G NCBI36
NG_009873.1:g.148793G>C
NG_009873.2:g.149386G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.4561-125G>C MANE Select ENSP00000262367.5:n.4561-125G>C
ENST00000262367.9:c.4561-125G>C ENSP00000262367.5:n.4561-125G>C
ENST00000382070.7:c.4447-125G>C ENSP00000371502.3:n.4447-125G>C
ENST00000570939.2:c.3196-125G>C ENSP00000461002.2:n.3196-125G>C
ENST00000571763.5:n.351-125G>C
ENST00000576720.1:n.3384-125G>C
NM_001079846.1:c.4447-125G>C NP_001073315.1:n.4447-125G>C
NM_004380.2:c.4561-125G>C NP_004371.2:n.4561-125G>C
XM_005255124.3:c.4516-125G>C XP_005255181.1:n.4516-125G>C
XM_005255125.3:c.4144-125G>C XP_005255182.1:n.4144-125G>C
XM_006720848.2:c.4300-125G>C XP_006720911.1:n.4300-125G>C
XM_011522380.1:c.4507-125G>C XP_011520682.1:n.4507-125G>C
XM_011522381.1:c.3808-125G>C XP_011520683.1:n.3808-125G>C
XM_005255124.4:c.4516-125G>C XP_005255181.1:n.4516-125G>C
XM_005255125.4:c.4144-125G>C XP_005255182.1:n.4144-125G>C
XM_006720848.3:c.4300-125G>C XP_006720911.1:n.4300-125G>C
XM_011522381.2:c.3808-125G>C XP_011520683.1:n.3808-125G>C
XM_017022944.1:c.4555-125G>C XP_016878433.1:n.4555-125G>C
NM_004380.3:c.4561-125G>C MANE Select NP_004371.2:n.4561-125G>C