Canonical Allele Identifier: CA394554198

Gene: CREBBP

Linked Data

• dbSNP Id: rs1158351339
• gnomAD v4: 16-3728936-C-A
• MyVariant Identifiers: chr16:g.3778937C>A (hg19) ; chr16:g.3728936C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728936C>A , CM000678.2:g.3728936C>A	GRCh38
NC_000016.9:g.3778937C>A , CM000678.1:g.3778937C>A	GRCh37
NC_000016.8:g.3718938C>A	NCBI36
NG_009873.1:g.156185G>T
NG_009873.2:g.156778G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000262367.10:c.6111G>T MANE Select	ENSP00000262367.5:p.Arg2037Ser
ENST00000262367.9:c.6111G>T	ENSP00000262367.5:p.Arg2037Ser
ENST00000382070.7:c.5997G>T	ENSP00000371502.3:p.Arg1999Ser
NM_001079846.1:c.5997G>T	NP_001073315.1:p.Arg1999Ser
NM_004380.2:c.6111G>T	NP_004371.2:p.Arg2037Ser
XM_005255124.3:c.6066G>T	XP_005255181.1:p.Arg2022Ser
XM_005255125.3:c.5694G>T	XP_005255182.1:p.Arg1898Ser
XM_006720848.2:c.5850G>T	XP_006720911.1:p.Arg1950Ser
XM_011522380.1:c.6057G>T	XP_011520682.1:p.Arg2019Ser
XM_011522381.1:c.5358G>T	XP_011520683.1:p.Arg1786Ser
XM_005255124.4:c.6066G>T	XP_005255181.1:p.Arg2022Ser
XM_005255125.4:c.5694G>T	XP_005255182.1:p.Arg1898Ser
XM_006720848.3:c.5850G>T	XP_006720911.1:p.Arg1950Ser
XM_011522381.2:c.5358G>T	XP_011520683.1:p.Arg1786Ser
XM_017022944.1:c.6105G>T	XP_016878433.1:p.Arg2035Ser
NM_004380.3:c.6111G>T MANE Select	NP_004371.2:p.Arg2037Ser