Canonical Allele Identifier: CA2631401944
Gene: CREBBP HGNC NCBI

Linked Data

gnomAD v4: 16-3737030-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3737030T>C , CM000678.2:g.3737030T>C GRCh38
NC_000016.9:g.3787031T>C , CM000678.1:g.3787031T>C GRCh37
NC_000016.8:g.3727032T>C NCBI36
NG_009873.1:g.148091A>G
NG_009873.2:g.148684A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.4395-215A>G MANE Select ENSP00000262367.5:n.4395-215A>G
ENST00000262367.9:c.4395-215A>G ENSP00000262367.5:n.4395-215A>G
ENST00000382070.7:c.4281-215A>G ENSP00000371502.3:n.4281-215A>G
ENST00000570939.2:c.3030-215A>G ENSP00000461002.2:n.3030-215A>G
ENST00000574740.1:n.216-215A>G
ENST00000576720.1:n.3218-215A>G
NM_001079846.1:c.4281-215A>G NP_001073315.1:n.4281-215A>G
NM_004380.2:c.4395-215A>G NP_004371.2:n.4395-215A>G
XM_005255124.3:c.4350-215A>G XP_005255181.1:n.4350-215A>G
XM_005255125.3:c.3978-215A>G XP_005255182.1:n.3978-215A>G
XM_006720848.2:c.4134-215A>G XP_006720911.1:n.4134-215A>G
XM_011522380.1:c.4341-215A>G XP_011520682.1:n.4341-215A>G
XM_011522381.1:c.3642-215A>G XP_011520683.1:n.3642-215A>G
XM_005255124.4:c.4350-215A>G XP_005255181.1:n.4350-215A>G
XM_005255125.4:c.3978-215A>G XP_005255182.1:n.3978-215A>G
XM_006720848.3:c.4134-215A>G XP_006720911.1:n.4134-215A>G
XM_011522381.2:c.3642-215A>G XP_011520683.1:n.3642-215A>G
XM_017022944.1:c.4389-215A>G XP_016878433.1:n.4389-215A>G
NM_004380.3:c.4395-215A>G MANE Select NP_004371.2:n.4395-215A>G