Canonical Allele Identifier: CA394550789

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151299795
• MyVariant Identifiers: chr16:g.3778026T>G (hg19) ; chr16:g.3728025T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728025T>G , CM000678.2:g.3728025T>G	GRCh38
NC_000016.9:g.3778026T>G , CM000678.1:g.3778026T>G	GRCh37
NC_000016.8:g.3718027T>G	NCBI36
NG_009873.1:g.157096A>C
NG_009873.2:g.157689A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.7022A>C MANE Select	ENSP00000262367.5:p.Asn2341Thr
ENST00000262367.9:c.7022A>C	ENSP00000262367.5:p.Asn2341Thr
ENST00000382070.7:c.6908A>C	ENSP00000371502.3:p.Asn2303Thr
NM_001079846.1:c.6908A>C	NP_001073315.1:p.Asn2303Thr
NM_004380.2:c.7022A>C	NP_004371.2:p.Asn2341Thr
XM_005255124.3:c.6977A>C	XP_005255181.1:p.Asn2326Thr
XM_005255125.3:c.6605A>C	XP_005255182.1:p.Asn2202Thr
XM_006720848.2:c.6761A>C	XP_006720911.1:p.Asn2254Thr
XM_011522380.1:c.6968A>C	XP_011520682.1:p.Asn2323Thr
XM_011522381.1:c.6269A>C	XP_011520683.1:p.Asn2090Thr
XM_005255124.4:c.6977A>C	XP_005255181.1:p.Asn2326Thr
XM_005255125.4:c.6605A>C	XP_005255182.1:p.Asn2202Thr
XM_006720848.3:c.6761A>C	XP_006720911.1:p.Asn2254Thr
XM_011522381.2:c.6269A>C	XP_011520683.1:p.Asn2090Thr
XM_017022944.1:c.7016A>C	XP_016878433.1:p.Asn2339Thr
NM_004380.3:c.7022A>C MANE Select	NP_004371.2:p.Asn2341Thr