Canonical Allele Identifier: CA493393449
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs2151299706
MyVariant Identifiers: chr16:g.3778013A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3728012A>T , CM000678.2:g.3728012A>T GRCh38
NC_000016.9:g.3778013A>T , CM000678.1:g.3778013A>T GRCh37
NC_000016.8:g.3718014A>T NCBI36
NG_009873.1:g.157109T>A
NG_009873.2:g.157702T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.7035T>A MANE Select ENSP00000262367.5:p.Ser2345=
ENST00000262367.9:c.7035T>A ENSP00000262367.5:p.Ser2345=
ENST00000382070.7:c.6921T>A ENSP00000371502.3:p.Ser2307=
NM_001079846.1:c.6921T>A NP_001073315.1:p.Ser2307=
NM_004380.2:c.7035T>A NP_004371.2:p.Ser2345=
XM_005255124.3:c.6990T>A XP_005255181.1:p.Ser2330=
XM_005255125.3:c.6618T>A XP_005255182.1:p.Ser2206=
XM_006720848.2:c.6774T>A XP_006720911.1:p.Ser2258=
XM_011522380.1:c.6981T>A XP_011520682.1:p.Ser2327=
XM_011522381.1:c.6282T>A XP_011520683.1:p.Ser2094=
XM_005255124.4:c.6990T>A XP_005255181.1:p.Ser2330=
XM_005255125.4:c.6618T>A XP_005255182.1:p.Ser2206=
XM_006720848.3:c.6774T>A XP_006720911.1:p.Ser2258=
XM_011522381.2:c.6282T>A XP_011520683.1:p.Ser2094=
XM_017022944.1:c.7029T>A XP_016878433.1:p.Ser2343=
NM_004380.3:c.7035T>A MANE Select NP_004371.2:p.Ser2345=