Canonical Allele Identifier: CA7868961
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs377597272
gnomAD v2: 16-3778024-G-A
gnomAD v3: 16-3728023-G-A
gnomAD v4: 16-3728023-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3728023G>A , CM000678.2:g.3728023G>A GRCh38
NC_000016.9:g.3778024G>A , CM000678.1:g.3778024G>A GRCh37
NC_000016.8:g.3718025G>A NCBI36
NG_009873.1:g.157098C>T
NG_009873.2:g.157691C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.7024C>T MANE Select ENSP00000262367.5:p.Gln2342Ter
ENST00000262367.9:c.7024C>T ENSP00000262367.5:p.Gln2342Ter
ENST00000382070.7:c.6910C>T ENSP00000371502.3:p.Gln2304Ter
NM_001079846.1:c.6910C>T NP_001073315.1:p.Gln2304Ter
NM_004380.2:c.7024C>T NP_004371.2:p.Gln2342Ter
XM_005255124.3:c.6979C>T XP_005255181.1:p.Gln2327Ter
XM_005255125.3:c.6607C>T XP_005255182.1:p.Gln2203Ter
XM_006720848.2:c.6763C>T XP_006720911.1:p.Gln2255Ter
XM_011522380.1:c.6970C>T XP_011520682.1:p.Gln2324Ter
XM_011522381.1:c.6271C>T XP_011520683.1:p.Gln2091Ter
XM_005255124.4:c.6979C>T XP_005255181.1:p.Gln2327Ter
XM_005255125.4:c.6607C>T XP_005255182.1:p.Gln2203Ter
XM_006720848.3:c.6763C>T XP_006720911.1:p.Gln2255Ter
XM_011522381.2:c.6271C>T XP_011520683.1:p.Gln2091Ter
XM_017022944.1:c.7018C>T XP_016878433.1:p.Gln2340Ter
NM_004380.3:c.7024C>T MANE Select NP_004371.2:p.Gln2342Ter