Canonical Allele Identifier: CA394551242

Gene: CREBBP

Linked Data

• dbSNP Id: rs1234402176
• MyVariant Identifiers: chr16:g.3778132C>A (hg19) ; chr16:g.3728131C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728131C>A , CM000678.2:g.3728131C>A	GRCh38
NC_000016.9:g.3778132C>A , CM000678.1:g.3778132C>A	GRCh37
NC_000016.8:g.3718133C>A	NCBI36
NG_009873.1:g.156990G>T
NG_009873.2:g.157583G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6916G>T MANE Select	ENSP00000262367.5:p.Gly2306Trp
ENST00000262367.9:c.6916G>T	ENSP00000262367.5:p.Gly2306Trp
ENST00000382070.7:c.6802G>T	ENSP00000371502.3:p.Gly2268Trp
NM_001079846.1:c.6802G>T	NP_001073315.1:p.Gly2268Trp
NM_004380.2:c.6916G>T	NP_004371.2:p.Gly2306Trp
XM_005255124.3:c.6871G>T	XP_005255181.1:p.Gly2291Trp
XM_005255125.3:c.6499G>T	XP_005255182.1:p.Gly2167Trp
XM_006720848.2:c.6655G>T	XP_006720911.1:p.Gly2219Trp
XM_011522380.1:c.6862G>T	XP_011520682.1:p.Gly2288Trp
XM_011522381.1:c.6163G>T	XP_011520683.1:p.Gly2055Trp
XM_005255124.4:c.6871G>T	XP_005255181.1:p.Gly2291Trp
XM_005255125.4:c.6499G>T	XP_005255182.1:p.Gly2167Trp
XM_006720848.3:c.6655G>T	XP_006720911.1:p.Gly2219Trp
XM_011522381.2:c.6163G>T	XP_011520683.1:p.Gly2055Trp
XM_017022944.1:c.6910G>T	XP_016878433.1:p.Gly2304Trp
NM_004380.3:c.6916G>T MANE Select	NP_004371.2:p.Gly2306Trp