Canonical Allele Identifier: CA493393658
Gene: CREBBP HGNC NCBI

Linked Data

dbSNP Id: rs2151305044
MyVariant Identifiers: chr16:g.3778778G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3728777G>A , CM000678.2:g.3728777G>A GRCh38
NC_000016.9:g.3778778G>A , CM000678.1:g.3778778G>A GRCh37
NC_000016.8:g.3718779G>A NCBI36
NG_009873.1:g.156344C>T
NG_009873.2:g.156937C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000262367.10:c.6270C>T MANE Select ENSP00000262367.5:p.Leu2090=
ENST00000262367.9:c.6270C>T ENSP00000262367.5:p.Leu2090=
ENST00000382070.7:c.6156C>T ENSP00000371502.3:p.Leu2052=
NM_001079846.1:c.6156C>T NP_001073315.1:p.Leu2052=
NM_004380.2:c.6270C>T NP_004371.2:p.Leu2090=
XM_005255124.3:c.6225C>T XP_005255181.1:p.Leu2075=
XM_005255125.3:c.5853C>T XP_005255182.1:p.Leu1951=
XM_006720848.2:c.6009C>T XP_006720911.1:p.Leu2003=
XM_011522380.1:c.6216C>T XP_011520682.1:p.Leu2072=
XM_011522381.1:c.5517C>T XP_011520683.1:p.Leu1839=
XM_005255124.4:c.6225C>T XP_005255181.1:p.Leu2075=
XM_005255125.4:c.5853C>T XP_005255182.1:p.Leu1951=
XM_006720848.3:c.6009C>T XP_006720911.1:p.Leu2003=
XM_011522381.2:c.5517C>T XP_011520683.1:p.Leu1839=
XM_017022944.1:c.6264C>T XP_016878433.1:p.Leu2088=
NM_004380.3:c.6270C>T MANE Select NP_004371.2:p.Leu2090=