Canonical Allele Identifier: CA620468487

Gene: CREBBP

Linked Data

• dbSNP Id: rs1393990509
• gnomAD v2: 16-3808817-C-A
• gnomAD v4: 16-3758816-C-A
• MyVariant Identifiers: chr16:g.3808817C>A (hg19) ; chr16:g.3758816C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3758816C>A , CM000678.2:g.3758816C>A	GRCh38
NC_000016.9:g.3808817C>A , CM000678.1:g.3808817C>A	GRCh37
NC_000016.8:g.3748818C>A	NCBI36
NG_009873.1:g.126305G>T
NG_009873.2:g.126898G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000262367.10:c.3369+38G>T MANE Select	ENSP00000262367.5:n.3369+38G>T
ENST00000262367.9:c.3369+38G>T	ENSP00000262367.5:n.3369+38G>T
ENST00000382070.7:c.3255+38G>T	ENSP00000371502.3:n.3255+38G>T
ENST00000570939.2:c.1974+38G>T	ENSP00000461002.2:n.1974+38G>T
NM_001079846.1:c.3255+38G>T	NP_001073315.1:n.3255+38G>T
NM_004380.2:c.3369+38G>T	NP_004371.2:n.3369+38G>T
XM_005255124.3:c.3324+38G>T	XP_005255181.1:n.3324+38G>T
XM_005255125.3:c.2952+38G>T	XP_005255182.1:n.2952+38G>T
XM_006720848.2:c.3369+38G>T	XP_006720911.1:n.3369+38G>T
XM_011522380.1:c.3315+38G>T	XP_011520682.1:n.3315+38G>T
XM_011522381.1:c.2616+38G>T	XP_011520683.1:n.2616+38G>T
XM_011522382.1:c.3369+38G>T	XP_011520684.1:n.3369+38G>T
XM_005255124.4:c.3324+38G>T	XP_005255181.1:n.3324+38G>T
XM_005255125.4:c.2952+38G>T	XP_005255182.1:n.2952+38G>T
XM_006720848.3:c.3369+38G>T	XP_006720911.1:n.3369+38G>T
XM_011522381.2:c.2616+38G>T	XP_011520683.1:n.2616+38G>T
XM_011522382.3:c.3369+38G>T	XP_011520684.1:n.3369+38G>T
XM_017022944.1:c.3363+38G>T	XP_016878433.1:n.3363+38G>T
NM_004380.3:c.3369+38G>T MANE Select	NP_004371.2:n.3369+38G>T