Canonical Allele Identifier: CA2731851229
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs2151312966

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3729912G>A , CM000678.2:g.3729912G>A GRCh38
NC_000016.9:g.3779913G>A , CM000678.1:g.3779913G>A GRCh37
NC_000016.8:g.3719914G>A NCBI36
NG_009873.1:g.155209C>T
NG_009873.2:g.155802C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.5173-38C>T MANE Select ENSP00000262367.5:n.5173-38C>T
ENST00000262367.9:c.5173-38C>T ENSP00000262367.5:n.5173-38C>T
ENST00000382070.7:c.5059-38C>T ENSP00000371502.3:n.5059-38C>T
NM_001079846.1:c.5059-38C>T NP_001073315.1:n.5059-38C>T
NM_004380.2:c.5173-38C>T NP_004371.2:n.5173-38C>T
XM_005255124.3:c.5128-38C>T XP_005255181.1:n.5128-38C>T
XM_005255125.3:c.4756-38C>T XP_005255182.1:n.4756-38C>T
XM_006720848.2:c.4912-38C>T XP_006720911.1:n.4912-38C>T
XM_011522380.1:c.5119-38C>T XP_011520682.1:n.5119-38C>T
XM_011522381.1:c.4420-38C>T XP_011520683.1:n.4420-38C>T
XM_005255124.4:c.5128-38C>T XP_005255181.1:n.5128-38C>T
XM_005255125.4:c.4756-38C>T XP_005255182.1:n.4756-38C>T
XM_006720848.3:c.4912-38C>T XP_006720911.1:n.4912-38C>T
XM_011522381.2:c.4420-38C>T XP_011520683.1:n.4420-38C>T
XM_017022944.1:c.5167-38C>T XP_016878433.1:n.5167-38C>T
NM_004380.3:c.5173-38C>T MANE Select NP_004371.2:n.5173-38C>T