Canonical Allele Identifier: CA394553921

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151305594
• MyVariant Identifiers: chr16:g.3778854C>G (hg19) ; chr16:g.3728853C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728853C>G , CM000678.2:g.3728853C>G	GRCh38
NC_000016.9:g.3778854C>G , CM000678.1:g.3778854C>G	GRCh37
NC_000016.8:g.3718855C>G	NCBI36
NG_009873.1:g.156268G>C
NG_009873.2:g.156861G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6194G>C MANE Select	ENSP00000262367.5:p.Ser2065Thr
ENST00000262367.9:c.6194G>C	ENSP00000262367.5:p.Ser2065Thr
ENST00000382070.7:c.6080G>C	ENSP00000371502.3:p.Ser2027Thr
NM_001079846.1:c.6080G>C	NP_001073315.1:p.Ser2027Thr
NM_004380.2:c.6194G>C	NP_004371.2:p.Ser2065Thr
XM_005255124.3:c.6149G>C	XP_005255181.1:p.Ser2050Thr
XM_005255125.3:c.5777G>C	XP_005255182.1:p.Ser1926Thr
XM_006720848.2:c.5933G>C	XP_006720911.1:p.Ser1978Thr
XM_011522380.1:c.6140G>C	XP_011520682.1:p.Ser2047Thr
XM_011522381.1:c.5441G>C	XP_011520683.1:p.Ser1814Thr
XM_005255124.4:c.6149G>C	XP_005255181.1:p.Ser2050Thr
XM_005255125.4:c.5777G>C	XP_005255182.1:p.Ser1926Thr
XM_006720848.3:c.5933G>C	XP_006720911.1:p.Ser1978Thr
XM_011522381.2:c.5441G>C	XP_011520683.1:p.Ser1814Thr
XM_017022944.1:c.6188G>C	XP_016878433.1:p.Ser2063Thr
NM_004380.3:c.6194G>C MANE Select	NP_004371.2:p.Ser2065Thr