Canonical Allele Identifier: CA394553947

Gene: CREBBP

Linked Data

• dbSNP Id: rs1317185442
• MyVariant Identifiers: chr16:g.3778866C>G (hg19) ; chr16:g.3728865C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728865C>G , CM000678.2:g.3728865C>G	GRCh38
NC_000016.9:g.3778866C>G , CM000678.1:g.3778866C>G	GRCh37
NC_000016.8:g.3718867C>G	NCBI36
NG_009873.1:g.156256G>C
NG_009873.2:g.156849G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6182G>C MANE Select	ENSP00000262367.5:p.Ser2061Thr
ENST00000262367.9:c.6182G>C	ENSP00000262367.5:p.Ser2061Thr
ENST00000382070.7:c.6068G>C	ENSP00000371502.3:p.Ser2023Thr
NM_001079846.1:c.6068G>C	NP_001073315.1:p.Ser2023Thr
NM_004380.2:c.6182G>C	NP_004371.2:p.Ser2061Thr
XM_005255124.3:c.6137G>C	XP_005255181.1:p.Ser2046Thr
XM_005255125.3:c.5765G>C	XP_005255182.1:p.Ser1922Thr
XM_006720848.2:c.5921G>C	XP_006720911.1:p.Ser1974Thr
XM_011522380.1:c.6128G>C	XP_011520682.1:p.Ser2043Thr
XM_011522381.1:c.5429G>C	XP_011520683.1:p.Ser1810Thr
XM_005255124.4:c.6137G>C	XP_005255181.1:p.Ser2046Thr
XM_005255125.4:c.5765G>C	XP_005255182.1:p.Ser1922Thr
XM_006720848.3:c.5921G>C	XP_006720911.1:p.Ser1974Thr
XM_011522381.2:c.5429G>C	XP_011520683.1:p.Ser1810Thr
XM_017022944.1:c.6176G>C	XP_016878433.1:p.Ser2059Thr
NM_004380.3:c.6182G>C MANE Select	NP_004371.2:p.Ser2061Thr