Canonical Allele Identifier: CA2631401353
Gene: CREBBP HGNC NCBI

Linked Data

gnomAD v4: 16-3736403-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3736403G>C , CM000678.2:g.3736403G>C GRCh38
NC_000016.9:g.3786404G>C , CM000678.1:g.3786404G>C GRCh37
NC_000016.8:g.3726405G>C NCBI36
NG_009873.1:g.148718C>G
NG_009873.2:g.149311C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.4561-200C>G MANE Select ENSP00000262367.5:n.4561-200C>G
ENST00000262367.9:c.4561-200C>G ENSP00000262367.5:n.4561-200C>G
ENST00000382070.7:c.4447-200C>G ENSP00000371502.3:n.4447-200C>G
ENST00000570939.2:c.3196-200C>G ENSP00000461002.2:n.3196-200C>G
ENST00000571763.5:n.351-200C>G
ENST00000576720.1:n.3384-200C>G
NM_001079846.1:c.4447-200C>G NP_001073315.1:n.4447-200C>G
NM_004380.2:c.4561-200C>G NP_004371.2:n.4561-200C>G
XM_005255124.3:c.4516-200C>G XP_005255181.1:n.4516-200C>G
XM_005255125.3:c.4144-200C>G XP_005255182.1:n.4144-200C>G
XM_006720848.2:c.4300-200C>G XP_006720911.1:n.4300-200C>G
XM_011522380.1:c.4507-200C>G XP_011520682.1:n.4507-200C>G
XM_011522381.1:c.3808-200C>G XP_011520683.1:n.3808-200C>G
XM_005255124.4:c.4516-200C>G XP_005255181.1:n.4516-200C>G
XM_005255125.4:c.4144-200C>G XP_005255182.1:n.4144-200C>G
XM_006720848.3:c.4300-200C>G XP_006720911.1:n.4300-200C>G
XM_011522381.2:c.3808-200C>G XP_011520683.1:n.3808-200C>G
XM_017022944.1:c.4555-200C>G XP_016878433.1:n.4555-200C>G
NM_004380.3:c.4561-200C>G MANE Select NP_004371.2:n.4561-200C>G