Canonical Allele Identifier: CA394554668

Gene: CREBBP

Linked Data

• dbSNP Id: rs1396077816
• MyVariant Identifiers: chr16:g.3779050G>C (hg19) ; chr16:g.3729049G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729049G>C , CM000678.2:g.3729049G>C	GRCh38
NC_000016.9:g.3779050G>C , CM000678.1:g.3779050G>C	GRCh37
NC_000016.8:g.3719051G>C	NCBI36
NG_009873.1:g.156072C>G
NG_009873.2:g.156665C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5998C>G MANE Select	ENSP00000262367.5:p.Leu2000Val
ENST00000262367.9:c.5998C>G	ENSP00000262367.5:p.Leu2000Val
ENST00000382070.7:c.5884C>G	ENSP00000371502.3:p.Leu1962Val
NM_001079846.1:c.5884C>G	NP_001073315.1:p.Leu1962Val
NM_004380.2:c.5998C>G	NP_004371.2:p.Leu2000Val
XM_005255124.3:c.5953C>G	XP_005255181.1:p.Leu1985Val
XM_005255125.3:c.5581C>G	XP_005255182.1:p.Leu1861Val
XM_006720848.2:c.5737C>G	XP_006720911.1:p.Leu1913Val
XM_011522380.1:c.5944C>G	XP_011520682.1:p.Leu1982Val
XM_011522381.1:c.5245C>G	XP_011520683.1:p.Leu1749Val
XM_005255124.4:c.5953C>G	XP_005255181.1:p.Leu1985Val
XM_005255125.4:c.5581C>G	XP_005255182.1:p.Leu1861Val
XM_006720848.3:c.5737C>G	XP_006720911.1:p.Leu1913Val
XM_011522381.2:c.5245C>G	XP_011520683.1:p.Leu1749Val
XM_017022944.1:c.5992C>G	XP_016878433.1:p.Leu1998Val
NM_004380.3:c.5998C>G MANE Select	NP_004371.2:p.Leu2000Val