Canonical Allele Identifier: CA493393272
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs1354388742
MyVariant Identifiers: chr16:g.3777887G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3727886G>T , CM000678.2:g.3727886G>T GRCh38
NC_000016.9:g.3777887G>T , CM000678.1:g.3777887G>T GRCh37
NC_000016.8:g.3717888G>T NCBI36
NG_009873.1:g.157235C>A
NG_009873.2:g.157828C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.7161C>A MANE Select ENSP00000262367.5:p.Leu2387=
ENST00000262367.9:c.7161C>A ENSP00000262367.5:p.Leu2387=
ENST00000382070.7:c.7047C>A ENSP00000371502.3:p.Leu2349=
NM_001079846.1:c.7047C>A NP_001073315.1:p.Leu2349=
NM_004380.2:c.7161C>A NP_004371.2:p.Leu2387=
XM_005255124.3:c.7116C>A XP_005255181.1:p.Leu2372=
XM_005255125.3:c.6744C>A XP_005255182.1:p.Leu2248=
XM_006720848.2:c.6900C>A XP_006720911.1:p.Leu2300=
XM_011522380.1:c.7107C>A XP_011520682.1:p.Leu2369=
XM_011522381.1:c.6408C>A XP_011520683.1:p.Leu2136=
XM_005255124.4:c.7116C>A XP_005255181.1:p.Leu2372=
XM_005255125.4:c.6744C>A XP_005255182.1:p.Leu2248=
XM_006720848.3:c.6900C>A XP_006720911.1:p.Leu2300=
XM_011522381.2:c.6408C>A XP_011520683.1:p.Leu2136=
XM_017022944.1:c.7155C>A XP_016878433.1:p.Leu2385=
NM_004380.3:c.7161C>A MANE Select NP_004371.2:p.Leu2387=