Canonical Allele Identifier: CA493393672

Gene: CREBBP

Linked Data

• gnomAD v4: 16-3728798-T-C
• MyVariant Identifiers: chr16:g.3778799T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728798T>C , CM000678.2:g.3728798T>C	GRCh38
NC_000016.9:g.3778799T>C , CM000678.1:g.3778799T>C	GRCh37
NC_000016.8:g.3718800T>C	NCBI36
NG_009873.1:g.156323A>G
NG_009873.2:g.156916A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6249A>G MANE Select	ENSP00000262367.5:p.Gln2083=
ENST00000262367.9:c.6249A>G	ENSP00000262367.5:p.Gln2083=
ENST00000382070.7:c.6135A>G	ENSP00000371502.3:p.Gln2045=
NM_001079846.1:c.6135A>G	NP_001073315.1:p.Gln2045=
NM_004380.2:c.6249A>G	NP_004371.2:p.Gln2083=
XM_005255124.3:c.6204A>G	XP_005255181.1:p.Gln2068=
XM_005255125.3:c.5832A>G	XP_005255182.1:p.Gln1944=
XM_006720848.2:c.5988A>G	XP_006720911.1:p.Gln1996=
XM_011522380.1:c.6195A>G	XP_011520682.1:p.Gln2065=
XM_011522381.1:c.5496A>G	XP_011520683.1:p.Gln1832=
XM_005255124.4:c.6204A>G	XP_005255181.1:p.Gln2068=
XM_005255125.4:c.5832A>G	XP_005255182.1:p.Gln1944=
XM_006720848.3:c.5988A>G	XP_006720911.1:p.Gln1996=
XM_011522381.2:c.5496A>G	XP_011520683.1:p.Gln1832=
XM_017022944.1:c.6243A>G	XP_016878433.1:p.Gln2081=
NM_004380.3:c.6249A>G MANE Select	NP_004371.2:p.Gln2083=