Canonical Allele Identifier: CA394557110

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151311580
• gnomAD v4: 16-3729706-G-A
• MyVariant Identifiers: chr16:g.3779707G>A (hg19) ; chr16:g.3729706G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729706G>A , CM000678.2:g.3729706G>A	GRCh38
NC_000016.9:g.3779707G>A , CM000678.1:g.3779707G>A	GRCh37
NC_000016.8:g.3719708G>A	NCBI36
NG_009873.1:g.155415C>T
NG_009873.2:g.156008C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5341C>T MANE Select	ENSP00000262367.5:p.His1781Tyr
ENST00000262367.9:c.5341C>T	ENSP00000262367.5:p.His1781Tyr
ENST00000382070.7:c.5227C>T	ENSP00000371502.3:p.His1743Tyr
NM_001079846.1:c.5227C>T	NP_001073315.1:p.His1743Tyr
NM_004380.2:c.5341C>T	NP_004371.2:p.His1781Tyr
XM_005255124.3:c.5296C>T	XP_005255181.1:p.His1766Tyr
XM_005255125.3:c.4924C>T	XP_005255182.1:p.His1642Tyr
XM_006720848.2:c.5080C>T	XP_006720911.1:p.His1694Tyr
XM_011522380.1:c.5287C>T	XP_011520682.1:p.His1763Tyr
XM_011522381.1:c.4588C>T	XP_011520683.1:p.His1530Tyr
XM_005255124.4:c.5296C>T	XP_005255181.1:p.His1766Tyr
XM_005255125.4:c.4924C>T	XP_005255182.1:p.His1642Tyr
XM_006720848.3:c.5080C>T	XP_006720911.1:p.His1694Tyr
XM_011522381.2:c.4588C>T	XP_011520683.1:p.His1530Tyr
XM_017022944.1:c.5335C>T	XP_016878433.1:p.His1779Tyr
NM_004380.3:c.5341C>T MANE Select	NP_004371.2:p.His1781Tyr