Canonical Allele Identifier: CA620459167

Gene: CREBBP

Linked Data

• ClinVar Variation Id: 1945961
• ClinVar RCV Id: RCV002680948
• dbSNP Id: rs1472959720
• gnomAD v2: 16-3827672-A-G
• gnomAD v4: 16-3777671-A-G
• MyVariant Identifiers: chr16:g.3827672A>G (hg19) ; chr16:g.3777671A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3777671A>G , CM000678.2:g.3777671A>G	GRCh38
NC_000016.9:g.3827672A>G , CM000678.1:g.3827672A>G	GRCh37
NC_000016.8:g.3767673A>G	NCBI36
NG_009873.1:g.107450T>C
NG_009873.2:g.108043T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000262367.10:c.2114-14T>C MANE Select	ENSP00000262367.5:n.2114-14T>C
ENST00000262367.9:c.2114-14T>C	ENSP00000262367.5:n.2114-14T>C
ENST00000382070.7:c.2000-14T>C	ENSP00000371502.3:n.2000-14T>C
ENST00000570939.2:c.719-14T>C	ENSP00000461002.2:n.719-14T>C
ENST00000571826.5:c.163-14T>C
ENST00000572134.1:c.426+340T>C
NM_001079846.1:c.2000-14T>C	NP_001073315.1:n.2000-14T>C
NM_004380.2:c.2114-14T>C	NP_004371.2:n.2114-14T>C
XM_005255124.3:c.2113+340T>C	XP_005255181.1:n.2113+340T>C
XM_005255125.3:c.2114-14T>C	XP_005255182.1:n.2114-14T>C
XM_006720848.2:c.2114-14T>C	XP_006720911.1:n.2114-14T>C
XM_011522380.1:c.2060-14T>C	XP_011520682.1:n.2060-14T>C
XM_011522381.1:c.1361-14T>C	XP_011520683.1:n.1361-14T>C
XM_011522382.1:c.2114-14T>C	XP_011520684.1:n.2114-14T>C
XM_005255124.4:c.2113+340T>C	XP_005255181.1:n.2113+340T>C
XM_005255125.4:c.2114-14T>C	XP_005255182.1:n.2114-14T>C
XM_006720848.3:c.2114-14T>C	XP_006720911.1:n.2114-14T>C
XM_011522381.2:c.1361-14T>C	XP_011520683.1:n.1361-14T>C
XM_011522382.3:c.2114-14T>C	XP_011520684.1:n.2114-14T>C
XM_017022944.1:c.2114-14T>C	XP_016878433.1:n.2114-14T>C
NM_004380.3:c.2114-14T>C MANE Select	NP_004371.2:n.2114-14T>C