Canonical Allele Identifier: CA394554026

Gene: CREBBP

Linked Data

• dbSNP Id: rs2051828003
• gnomAD v3: 16-3728887-G-A
• gnomAD v4: 16-3728887-G-A
• MyVariant Identifiers: chr16:g.3778888G>A (hg19) ; chr16:g.3728887G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728887G>A , CM000678.2:g.3728887G>A	GRCh38
NC_000016.9:g.3778888G>A , CM000678.1:g.3778888G>A	GRCh37
NC_000016.8:g.3718889G>A	NCBI36
NG_009873.1:g.156234C>T
NG_009873.2:g.156827C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6160C>T MANE Select	ENSP00000262367.5:p.Pro2054Ser
ENST00000262367.9:c.6160C>T	ENSP00000262367.5:p.Pro2054Ser
ENST00000382070.7:c.6046C>T	ENSP00000371502.3:p.Pro2016Ser
NM_001079846.1:c.6046C>T	NP_001073315.1:p.Pro2016Ser
NM_004380.2:c.6160C>T	NP_004371.2:p.Pro2054Ser
XM_005255124.3:c.6115C>T	XP_005255181.1:p.Pro2039Ser
XM_005255125.3:c.5743C>T	XP_005255182.1:p.Pro1915Ser
XM_006720848.2:c.5899C>T	XP_006720911.1:p.Pro1967Ser
XM_011522380.1:c.6106C>T	XP_011520682.1:p.Pro2036Ser
XM_011522381.1:c.5407C>T	XP_011520683.1:p.Pro1803Ser
XM_005255124.4:c.6115C>T	XP_005255181.1:p.Pro2039Ser
XM_005255125.4:c.5743C>T	XP_005255182.1:p.Pro1915Ser
XM_006720848.3:c.5899C>T	XP_006720911.1:p.Pro1967Ser
XM_011522381.2:c.5407C>T	XP_011520683.1:p.Pro1803Ser
XM_017022944.1:c.6154C>T	XP_016878433.1:p.Pro2052Ser
NM_004380.3:c.6160C>T MANE Select	NP_004371.2:p.Pro2054Ser