Canonical Allele Identifier: CA394554808

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151307028
• gnomAD v4: 16-3729083-C-A
• MyVariant Identifiers: chr16:g.3779084C>A (hg19) ; chr16:g.3729083C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3729083C>A , CM000678.2:g.3729083C>A	GRCh38
NC_000016.9:g.3779084C>A , CM000678.1:g.3779084C>A	GRCh37
NC_000016.8:g.3719085C>A	NCBI36
NG_009873.1:g.156038G>T
NG_009873.2:g.156631G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.5964G>T MANE Select	ENSP00000262367.5:p.Met1988Ile
ENST00000262367.9:c.5964G>T	ENSP00000262367.5:p.Met1988Ile
ENST00000382070.7:c.5850G>T	ENSP00000371502.3:p.Met1950Ile
NM_001079846.1:c.5850G>T	NP_001073315.1:p.Met1950Ile
NM_004380.2:c.5964G>T	NP_004371.2:p.Met1988Ile
XM_005255124.3:c.5919G>T	XP_005255181.1:p.Met1973Ile
XM_005255125.3:c.5547G>T	XP_005255182.1:p.Met1849Ile
XM_006720848.2:c.5703G>T	XP_006720911.1:p.Met1901Ile
XM_011522380.1:c.5910G>T	XP_011520682.1:p.Met1970Ile
XM_011522381.1:c.5211G>T	XP_011520683.1:p.Met1737Ile
XM_005255124.4:c.5919G>T	XP_005255181.1:p.Met1973Ile
XM_005255125.4:c.5547G>T	XP_005255182.1:p.Met1849Ile
XM_006720848.3:c.5703G>T	XP_006720911.1:p.Met1901Ile
XM_011522381.2:c.5211G>T	XP_011520683.1:p.Met1737Ile
XM_017022944.1:c.5958G>T	XP_016878433.1:p.Met1986Ile
NM_004380.3:c.5964G>T MANE Select	NP_004371.2:p.Met1988Ile