Canonical Allele Identifier: CA394554958

Gene: CREBBP

Linked Data

• dbSNP Id: rs1163626684
• MyVariant Identifiers: chr16:g.3779121T>A (hg19) ; chr16:g.3729120T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729120T>A , CM000678.2:g.3729120T>A	GRCh38
NC_000016.9:g.3779121T>A , CM000678.1:g.3779121T>A	GRCh37
NC_000016.8:g.3719122T>A	NCBI36
NG_009873.1:g.156001A>T
NG_009873.2:g.156594A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5927A>T MANE Select	ENSP00000262367.5:p.Asn1976Ile
ENST00000262367.9:c.5927A>T	ENSP00000262367.5:p.Asn1976Ile
ENST00000382070.7:c.5813A>T	ENSP00000371502.3:p.Asn1938Ile
NM_001079846.1:c.5813A>T	NP_001073315.1:p.Asn1938Ile
NM_004380.2:c.5927A>T	NP_004371.2:p.Asn1976Ile
XM_005255124.3:c.5882A>T	XP_005255181.1:p.Asn1961Ile
XM_005255125.3:c.5510A>T	XP_005255182.1:p.Asn1837Ile
XM_006720848.2:c.5666A>T	XP_006720911.1:p.Asn1889Ile
XM_011522380.1:c.5873A>T	XP_011520682.1:p.Asn1958Ile
XM_011522381.1:c.5174A>T	XP_011520683.1:p.Asn1725Ile
XM_005255124.4:c.5882A>T	XP_005255181.1:p.Asn1961Ile
XM_005255125.4:c.5510A>T	XP_005255182.1:p.Asn1837Ile
XM_006720848.3:c.5666A>T	XP_006720911.1:p.Asn1889Ile
XM_011522381.2:c.5174A>T	XP_011520683.1:p.Asn1725Ile
XM_017022944.1:c.5921A>T	XP_016878433.1:p.Asn1974Ile
NM_004380.3:c.5927A>T MANE Select	NP_004371.2:p.Asn1976Ile