Canonical Allele Identifier: CA394550671

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151299566
• MyVariant Identifiers: chr16:g.3777994G>T (hg19) ; chr16:g.3727993G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3727993G>T , CM000678.2:g.3727993G>T	GRCh38
NC_000016.9:g.3777994G>T , CM000678.1:g.3777994G>T	GRCh37
NC_000016.8:g.3717995G>T	NCBI36
NG_009873.1:g.157128C>A
NG_009873.2:g.157721C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.7054C>A MANE Select	ENSP00000262367.5:p.Pro2352Thr
ENST00000262367.9:c.7054C>A	ENSP00000262367.5:p.Pro2352Thr
ENST00000382070.7:c.6940C>A	ENSP00000371502.3:p.Pro2314Thr
NM_001079846.1:c.6940C>A	NP_001073315.1:p.Pro2314Thr
NM_004380.2:c.7054C>A	NP_004371.2:p.Pro2352Thr
XM_005255124.3:c.7009C>A	XP_005255181.1:p.Pro2337Thr
XM_005255125.3:c.6637C>A	XP_005255182.1:p.Pro2213Thr
XM_006720848.2:c.6793C>A	XP_006720911.1:p.Pro2265Thr
XM_011522380.1:c.7000C>A	XP_011520682.1:p.Pro2334Thr
XM_011522381.1:c.6301C>A	XP_011520683.1:p.Pro2101Thr
XM_005255124.4:c.7009C>A	XP_005255181.1:p.Pro2337Thr
XM_005255125.4:c.6637C>A	XP_005255182.1:p.Pro2213Thr
XM_006720848.3:c.6793C>A	XP_006720911.1:p.Pro2265Thr
XM_011522381.2:c.6301C>A	XP_011520683.1:p.Pro2101Thr
XM_017022944.1:c.7048C>A	XP_016878433.1:p.Pro2350Thr
NM_004380.3:c.7054C>A MANE Select	NP_004371.2:p.Pro2352Thr