Canonical Allele Identifier: CA2631399177
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs2051866366
gnomAD v4: 16-3729926-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3729926C>G , CM000678.2:g.3729926C>G GRCh38
NC_000016.9:g.3779927C>G , CM000678.1:g.3779927C>G GRCh37
NC_000016.8:g.3719928C>G NCBI36
NG_009873.1:g.155195G>C
NG_009873.2:g.155788G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.5173-52G>C MANE Select ENSP00000262367.5:n.5173-52G>C
ENST00000262367.9:c.5173-52G>C ENSP00000262367.5:n.5173-52G>C
ENST00000382070.7:c.5059-52G>C ENSP00000371502.3:n.5059-52G>C
NM_001079846.1:c.5059-52G>C NP_001073315.1:n.5059-52G>C
NM_004380.2:c.5173-52G>C NP_004371.2:n.5173-52G>C
XM_005255124.3:c.5128-52G>C XP_005255181.1:n.5128-52G>C
XM_005255125.3:c.4756-52G>C XP_005255182.1:n.4756-52G>C
XM_006720848.2:c.4912-52G>C XP_006720911.1:n.4912-52G>C
XM_011522380.1:c.5119-52G>C XP_011520682.1:n.5119-52G>C
XM_011522381.1:c.4420-52G>C XP_011520683.1:n.4420-52G>C
XM_005255124.4:c.5128-52G>C XP_005255181.1:n.5128-52G>C
XM_005255125.4:c.4756-52G>C XP_005255182.1:n.4756-52G>C
XM_006720848.3:c.4912-52G>C XP_006720911.1:n.4912-52G>C
XM_011522381.2:c.4420-52G>C XP_011520683.1:n.4420-52G>C
XM_017022944.1:c.5167-52G>C XP_016878433.1:n.5167-52G>C
NM_004380.3:c.5173-52G>C MANE Select NP_004371.2:n.5173-52G>C