Canonical Allele Identifier: CA394551025

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151300148
• MyVariant Identifiers: chr16:g.3778083G>C (hg19) ; chr16:g.3728082G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728082G>C , CM000678.2:g.3728082G>C	GRCh38
NC_000016.9:g.3778083G>C , CM000678.1:g.3778083G>C	GRCh37
NC_000016.8:g.3718084G>C	NCBI36
NG_009873.1:g.157039C>G
NG_009873.2:g.157632C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6965C>G MANE Select	ENSP00000262367.5:p.Ser2322Ter
ENST00000262367.9:c.6965C>G	ENSP00000262367.5:p.Ser2322Ter
ENST00000382070.7:c.6851C>G	ENSP00000371502.3:p.Ser2284Ter
NM_001079846.1:c.6851C>G	NP_001073315.1:p.Ser2284Ter
NM_004380.2:c.6965C>G	NP_004371.2:p.Ser2322Ter
XM_005255124.3:c.6920C>G	XP_005255181.1:p.Ser2307Ter
XM_005255125.3:c.6548C>G	XP_005255182.1:p.Ser2183Ter
XM_006720848.2:c.6704C>G	XP_006720911.1:p.Ser2235Ter
XM_011522380.1:c.6911C>G	XP_011520682.1:p.Ser2304Ter
XM_011522381.1:c.6212C>G	XP_011520683.1:p.Ser2071Ter
XM_005255124.4:c.6920C>G	XP_005255181.1:p.Ser2307Ter
XM_005255125.4:c.6548C>G	XP_005255182.1:p.Ser2183Ter
XM_006720848.3:c.6704C>G	XP_006720911.1:p.Ser2235Ter
XM_011522381.2:c.6212C>G	XP_011520683.1:p.Ser2071Ter
XM_017022944.1:c.6959C>G	XP_016878433.1:p.Ser2320Ter
NM_004380.3:c.6965C>G MANE Select	NP_004371.2:p.Ser2322Ter