Canonical Allele Identifier: CA394554438

Gene: CREBBP

Linked Data

• dbSNP Id: rs368367342
• gnomAD v4: 16-3728997-G-C
• MyVariant Identifiers: chr16:g.3778998G>C (hg19) ; chr16:g.3728997G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728997G>C , CM000678.2:g.3728997G>C	GRCh38
NC_000016.9:g.3778998G>C , CM000678.1:g.3778998G>C	GRCh37
NC_000016.8:g.3718999G>C	NCBI36
NG_009873.1:g.156124C>G
NG_009873.2:g.156717C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6050C>G MANE Select	ENSP00000262367.5:p.Pro2017Arg
ENST00000262367.9:c.6050C>G	ENSP00000262367.5:p.Pro2017Arg
ENST00000382070.7:c.5936C>G	ENSP00000371502.3:p.Pro1979Arg
NM_001079846.1:c.5936C>G	NP_001073315.1:p.Pro1979Arg
NM_004380.2:c.6050C>G	NP_004371.2:p.Pro2017Arg
XM_005255124.3:c.6005C>G	XP_005255181.1:p.Pro2002Arg
XM_005255125.3:c.5633C>G	XP_005255182.1:p.Pro1878Arg
XM_006720848.2:c.5789C>G	XP_006720911.1:p.Pro1930Arg
XM_011522380.1:c.5996C>G	XP_011520682.1:p.Pro1999Arg
XM_011522381.1:c.5297C>G	XP_011520683.1:p.Pro1766Arg
XM_005255124.4:c.6005C>G	XP_005255181.1:p.Pro2002Arg
XM_005255125.4:c.5633C>G	XP_005255182.1:p.Pro1878Arg
XM_006720848.3:c.5789C>G	XP_006720911.1:p.Pro1930Arg
XM_011522381.2:c.5297C>G	XP_011520683.1:p.Pro1766Arg
XM_017022944.1:c.6044C>G	XP_016878433.1:p.Pro2015Arg
NM_004380.3:c.6050C>G MANE Select	NP_004371.2:p.Pro2017Arg