Canonical Allele Identifier: CA394553911

Gene: CREBBP

Linked Data

• dbSNP Id: rs1442302909
• gnomAD v2: 16-3778849-G-C
• gnomAD v4: 16-3728848-G-C
• MyVariant Identifiers: chr16:g.3778849G>C (hg19) ; chr16:g.3728848G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728848G>C , CM000678.2:g.3728848G>C	GRCh38
NC_000016.9:g.3778849G>C , CM000678.1:g.3778849G>C	GRCh37
NC_000016.8:g.3718850G>C	NCBI36
NG_009873.1:g.156273C>G
NG_009873.2:g.156866C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6199C>G MANE Select	ENSP00000262367.5:p.Leu2067Val
ENST00000262367.9:c.6199C>G	ENSP00000262367.5:p.Leu2067Val
ENST00000382070.7:c.6085C>G	ENSP00000371502.3:p.Leu2029Val
NM_001079846.1:c.6085C>G	NP_001073315.1:p.Leu2029Val
NM_004380.2:c.6199C>G	NP_004371.2:p.Leu2067Val
XM_005255124.3:c.6154C>G	XP_005255181.1:p.Leu2052Val
XM_005255125.3:c.5782C>G	XP_005255182.1:p.Leu1928Val
XM_006720848.2:c.5938C>G	XP_006720911.1:p.Leu1980Val
XM_011522380.1:c.6145C>G	XP_011520682.1:p.Leu2049Val
XM_011522381.1:c.5446C>G	XP_011520683.1:p.Leu1816Val
XM_005255124.4:c.6154C>G	XP_005255181.1:p.Leu2052Val
XM_005255125.4:c.5782C>G	XP_005255182.1:p.Leu1928Val
XM_006720848.3:c.5938C>G	XP_006720911.1:p.Leu1980Val
XM_011522381.2:c.5446C>G	XP_011520683.1:p.Leu1816Val
XM_017022944.1:c.6193C>G	XP_016878433.1:p.Leu2065Val
NM_004380.3:c.6199C>G MANE Select	NP_004371.2:p.Leu2067Val