Canonical Allele Identifier: CA276988149
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs555765549
gnomAD v2: 16-3796088-G-A
gnomAD v3: 16-3746087-G-A
gnomAD v4: 16-3746087-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3746087G>A , CM000678.2:g.3746087G>A GRCh38
NC_000016.9:g.3796088G>A , CM000678.1:g.3796088G>A GRCh37
NC_000016.8:g.3736089G>A NCBI36
NG_009873.1:g.139034C>T
NG_009873.2:g.139627C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000262367.10:c.3837-733C>T MANE Select ENSP00000262367.5:n.3837-733C>T
ENST00000638158.1:n.58-492C>T
ENST00000262367.9:c.3837-733C>T ENSP00000262367.5:n.3837-733C>T
ENST00000382070.7:c.3723-733C>T ENSP00000371502.3:n.3723-733C>T
ENST00000570939.2:c.2472-733C>T ENSP00000461002.2:n.2472-733C>T
ENST00000573517.6:c.143-733C>T
NM_001079846.1:c.3723-733C>T NP_001073315.1:n.3723-733C>T
NM_004380.2:c.3837-733C>T NP_004371.2:n.3837-733C>T
XM_005255124.3:c.3792-733C>T XP_005255181.1:n.3792-733C>T
XM_005255125.3:c.3420-733C>T XP_005255182.1:n.3420-733C>T
XM_006720848.2:c.3837-733C>T XP_006720911.1:n.3837-733C>T
XM_011522380.1:c.3783-733C>T XP_011520682.1:n.3783-733C>T
XM_011522381.1:c.3084-733C>T XP_011520683.1:n.3084-733C>T
XM_011522382.1:c.3837-492C>T XP_011520684.1:n.3837-492C>T
XM_005255124.4:c.3792-733C>T XP_005255181.1:n.3792-733C>T
XM_005255125.4:c.3420-733C>T XP_005255182.1:n.3420-733C>T
XM_006720848.3:c.3837-733C>T XP_006720911.1:n.3837-733C>T
XM_011522381.2:c.3084-733C>T XP_011520683.1:n.3084-733C>T
XM_011522382.3:c.3837-492C>T XP_011520684.1:n.3837-492C>T
XM_017022944.1:c.3831-733C>T XP_016878433.1:n.3831-733C>T
NM_004380.3:c.3837-733C>T MANE Select NP_004371.2:n.3837-733C>T