Canonical Allele Identifier: CA620462610

Gene: CREBBP

Linked Data

• dbSNP Id: rs1362659887
• gnomAD v2: 16-3841952-C-G
• gnomAD v4: 16-3791951-C-G
• MyVariant Identifiers: chr16:g.3841952C>G (hg19) ; chr16:g.3791951C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3791951C>G , CM000678.2:g.3791951C>G	GRCh38
NC_000016.9:g.3841952C>G , CM000678.1:g.3841952C>G	GRCh37
NC_000016.8:g.3781953C>G	NCBI36
NG_009873.1:g.93170G>C
NG_009873.2:g.93763G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000262367.10:c.1330+30G>C MANE Select	ENSP00000262367.5:n.1330+30G>C
ENST00000262367.9:c.1330+30G>C	ENSP00000262367.5:n.1330+30G>C
ENST00000382070.7:c.1216+1435G>C	ENSP00000371502.3:n.1216+1435G>C
NM_001079846.1:c.1216+1435G>C	NP_001073315.1:n.1216+1435G>C
NM_004380.2:c.1330+30G>C	NP_004371.2:n.1330+30G>C
XM_005255124.3:c.1330+30G>C	XP_005255181.1:n.1330+30G>C
XM_005255125.3:c.1330+30G>C	XP_005255182.1:n.1330+30G>C
XM_006720848.2:c.1330+30G>C	XP_006720911.1:n.1330+30G>C
XM_011522380.1:c.1276+30G>C	XP_011520682.1:n.1276+30G>C
XM_011522381.1:c.577+30G>C	XP_011520683.1:n.577+30G>C
XM_011522382.1:c.1330+30G>C	XP_011520684.1:n.1330+30G>C
XM_005255124.4:c.1330+30G>C	XP_005255181.1:n.1330+30G>C
XM_005255125.4:c.1330+30G>C	XP_005255182.1:n.1330+30G>C
XM_006720848.3:c.1330+30G>C	XP_006720911.1:n.1330+30G>C
XM_011522381.2:c.577+30G>C	XP_011520683.1:n.577+30G>C
XM_011522382.3:c.1330+30G>C	XP_011520684.1:n.1330+30G>C
XM_017022944.1:c.1330+30G>C	XP_016878433.1:n.1330+30G>C
NM_004380.3:c.1330+30G>C MANE Select	NP_004371.2:n.1330+30G>C