Canonical Allele Identifier: CA277007689

Gene: CREBBP

Linked Data

• dbSNP Id: rs928179865
• gnomAD v4: 16-3810572-G-A
• MyVariant Identifiers: chr16:g.3860573G>A (hg19) ; chr16:g.3810572G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3810572G>A , CM000678.2:g.3810572G>A	GRCh38
NC_000016.9:g.3860573G>A , CM000678.1:g.3860573G>A	GRCh37
NC_000016.8:g.3800574G>A	NCBI36
NG_009873.1:g.74549C>T
NG_009873.2:g.75142C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.975+31C>T MANE Select	ENSP00000262367.5:n.975+31C>T
ENST00000262367.9:c.975+31C>T	ENSP00000262367.5:n.975+31C>T
ENST00000382070.7:c.975+31C>T	ENSP00000371502.3:n.975+31C>T
NM_001079846.1:c.975+31C>T	NP_001073315.1:n.975+31C>T
NM_004380.2:c.975+31C>T	NP_004371.2:n.975+31C>T
XM_005255124.3:c.975+31C>T	XP_005255181.1:n.975+31C>T
XM_005255125.3:c.975+31C>T	XP_005255182.1:n.975+31C>T
XM_006720848.2:c.975+31C>T	XP_006720911.1:n.975+31C>T
XM_011522380.1:c.921+31C>T	XP_011520682.1:n.921+31C>T
XM_011522381.1:c.222+31C>T	XP_011520683.1:n.222+31C>T
XM_011522382.1:c.975+31C>T	XP_011520684.1:n.975+31C>T
XM_005255124.4:c.975+31C>T	XP_005255181.1:n.975+31C>T
XM_005255125.4:c.975+31C>T	XP_005255182.1:n.975+31C>T
XM_006720848.3:c.975+31C>T	XP_006720911.1:n.975+31C>T
XM_011522381.2:c.222+31C>T	XP_011520683.1:n.222+31C>T
XM_011522382.3:c.975+31C>T	XP_011520684.1:n.975+31C>T
XM_017022944.1:c.975+31C>T	XP_016878433.1:n.975+31C>T
NM_004380.3:c.975+31C>T MANE Select	NP_004371.2:n.975+31C>T