Canonical Allele Identifier: CA394556138

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151310236
• gnomAD v4: 16-3729532-G-A
• MyVariant Identifiers: chr16:g.3779533G>A (hg19) ; chr16:g.3729532G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729532G>A , CM000678.2:g.3729532G>A	GRCh38
NC_000016.9:g.3779533G>A , CM000678.1:g.3779533G>A	GRCh37
NC_000016.8:g.3719534G>A	NCBI36
NG_009873.1:g.155589C>T
NG_009873.2:g.156182C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5515C>T MANE Select	ENSP00000262367.5:p.Pro1839Ser
ENST00000262367.9:c.5515C>T	ENSP00000262367.5:p.Pro1839Ser
ENST00000382070.7:c.5401C>T	ENSP00000371502.3:p.Pro1801Ser
NM_001079846.1:c.5401C>T	NP_001073315.1:p.Pro1801Ser
NM_004380.2:c.5515C>T	NP_004371.2:p.Pro1839Ser
XM_005255124.3:c.5470C>T	XP_005255181.1:p.Pro1824Ser
XM_005255125.3:c.5098C>T	XP_005255182.1:p.Pro1700Ser
XM_006720848.2:c.5254C>T	XP_006720911.1:p.Pro1752Ser
XM_011522380.1:c.5461C>T	XP_011520682.1:p.Pro1821Ser
XM_011522381.1:c.4762C>T	XP_011520683.1:p.Pro1588Ser
XM_005255124.4:c.5470C>T	XP_005255181.1:p.Pro1824Ser
XM_005255125.4:c.5098C>T	XP_005255182.1:p.Pro1700Ser
XM_006720848.3:c.5254C>T	XP_006720911.1:p.Pro1752Ser
XM_011522381.2:c.4762C>T	XP_011520683.1:p.Pro1588Ser
XM_017022944.1:c.5509C>T	XP_016878433.1:p.Pro1837Ser
NM_004380.3:c.5515C>T MANE Select	NP_004371.2:p.Pro1839Ser