Canonical Allele Identifier: CA394551147

Gene: CREBBP

Linked Data

• dbSNP Id: rs979662378
• MyVariant Identifiers: chr16:g.3778108T>A (hg19) ; chr16:g.3728107T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728107T>A , CM000678.2:g.3728107T>A	GRCh38
NC_000016.9:g.3778108T>A , CM000678.1:g.3778108T>A	GRCh37
NC_000016.8:g.3718109T>A	NCBI36
NG_009873.1:g.157014A>T
NG_009873.2:g.157607A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262367.10:c.6940A>T MANE Select	ENSP00000262367.5:p.Met2314Leu
ENST00000262367.9:c.6940A>T	ENSP00000262367.5:p.Met2314Leu
ENST00000382070.7:c.6826A>T	ENSP00000371502.3:p.Met2276Leu
NM_001079846.1:c.6826A>T	NP_001073315.1:p.Met2276Leu
NM_004380.2:c.6940A>T	NP_004371.2:p.Met2314Leu
XM_005255124.3:c.6895A>T	XP_005255181.1:p.Met2299Leu
XM_005255125.3:c.6523A>T	XP_005255182.1:p.Met2175Leu
XM_006720848.2:c.6679A>T	XP_006720911.1:p.Met2227Leu
XM_011522380.1:c.6886A>T	XP_011520682.1:p.Met2296Leu
XM_011522381.1:c.6187A>T	XP_011520683.1:p.Met2063Leu
XM_005255124.4:c.6895A>T	XP_005255181.1:p.Met2299Leu
XM_005255125.4:c.6523A>T	XP_005255182.1:p.Met2175Leu
XM_006720848.3:c.6679A>T	XP_006720911.1:p.Met2227Leu
XM_011522381.2:c.6187A>T	XP_011520683.1:p.Met2063Leu
XM_017022944.1:c.6934A>T	XP_016878433.1:p.Met2312Leu
NM_004380.3:c.6940A>T MANE Select	NP_004371.2:p.Met2314Leu