Canonical Allele Identifier: CA394556591

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151311179
• MyVariant Identifiers: chr16:g.3779655A>C (hg19) ; chr16:g.3729654A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729654A>C , CM000678.2:g.3729654A>C	GRCh38
NC_000016.9:g.3779655A>C , CM000678.1:g.3779655A>C	GRCh37
NC_000016.8:g.3719656A>C	NCBI36
NG_009873.1:g.155467T>G
NG_009873.2:g.156060T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5393T>G MANE Select	ENSP00000262367.5:p.Met1798Arg
ENST00000262367.9:c.5393T>G	ENSP00000262367.5:p.Met1798Arg
ENST00000382070.7:c.5279T>G	ENSP00000371502.3:p.Met1760Arg
NM_001079846.1:c.5279T>G	NP_001073315.1:p.Met1760Arg
NM_004380.2:c.5393T>G	NP_004371.2:p.Met1798Arg
XM_005255124.3:c.5348T>G	XP_005255181.1:p.Met1783Arg
XM_005255125.3:c.4976T>G	XP_005255182.1:p.Met1659Arg
XM_006720848.2:c.5132T>G	XP_006720911.1:p.Met1711Arg
XM_011522380.1:c.5339T>G	XP_011520682.1:p.Met1780Arg
XM_011522381.1:c.4640T>G	XP_011520683.1:p.Met1547Arg
XM_005255124.4:c.5348T>G	XP_005255181.1:p.Met1783Arg
XM_005255125.4:c.4976T>G	XP_005255182.1:p.Met1659Arg
XM_006720848.3:c.5132T>G	XP_006720911.1:p.Met1711Arg
XM_011522381.2:c.4640T>G	XP_011520683.1:p.Met1547Arg
XM_017022944.1:c.5387T>G	XP_016878433.1:p.Met1796Arg
NM_004380.3:c.5393T>G MANE Select	NP_004371.2:p.Met1798Arg