Canonical Allele Identifier: CA493393724

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151305598
• MyVariant Identifiers: chr16:g.3778856G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728855G>C , CM000678.2:g.3728855G>C	GRCh38
NC_000016.9:g.3778856G>C , CM000678.1:g.3778856G>C	GRCh37
NC_000016.8:g.3718857G>C	NCBI36
NG_009873.1:g.156266C>G
NG_009873.2:g.156859C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6192C>G MANE Select	ENSP00000262367.5:p.Pro2064=
ENST00000262367.9:c.6192C>G	ENSP00000262367.5:p.Pro2064=
ENST00000382070.7:c.6078C>G	ENSP00000371502.3:p.Pro2026=
NM_001079846.1:c.6078C>G	NP_001073315.1:p.Pro2026=
NM_004380.2:c.6192C>G	NP_004371.2:p.Pro2064=
XM_005255124.3:c.6147C>G	XP_005255181.1:p.Pro2049=
XM_005255125.3:c.5775C>G	XP_005255182.1:p.Pro1925=
XM_006720848.2:c.5931C>G	XP_006720911.1:p.Pro1977=
XM_011522380.1:c.6138C>G	XP_011520682.1:p.Pro2046=
XM_011522381.1:c.5439C>G	XP_011520683.1:p.Pro1813=
XM_005255124.4:c.6147C>G	XP_005255181.1:p.Pro2049=
XM_005255125.4:c.5775C>G	XP_005255182.1:p.Pro1925=
XM_006720848.3:c.5931C>G	XP_006720911.1:p.Pro1977=
XM_011522381.2:c.5439C>G	XP_011520683.1:p.Pro1813=
XM_017022944.1:c.6186C>G	XP_016878433.1:p.Pro2062=
NM_004380.3:c.6192C>G MANE Select	NP_004371.2:p.Pro2064=