Canonical Allele Identifier: CA394554196

Gene: CREBBP

Linked Data

• dbSNP Id: rs2151306093
• MyVariant Identifiers: chr16:g.3778936G>C (hg19) ; chr16:g.3728935G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3728935G>C , CM000678.2:g.3728935G>C	GRCh38
NC_000016.9:g.3778936G>C , CM000678.1:g.3778936G>C	GRCh37
NC_000016.8:g.3718937G>C	NCBI36
NG_009873.1:g.156186C>G
NG_009873.2:g.156779C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000262367.10:c.6112C>G MANE Select	ENSP00000262367.5:p.Pro2038Ala
ENST00000262367.9:c.6112C>G	ENSP00000262367.5:p.Pro2038Ala
ENST00000382070.7:c.5998C>G	ENSP00000371502.3:p.Pro2000Ala
NM_001079846.1:c.5998C>G	NP_001073315.1:p.Pro2000Ala
NM_004380.2:c.6112C>G	NP_004371.2:p.Pro2038Ala
XM_005255124.3:c.6067C>G	XP_005255181.1:p.Pro2023Ala
XM_005255125.3:c.5695C>G	XP_005255182.1:p.Pro1899Ala
XM_006720848.2:c.5851C>G	XP_006720911.1:p.Pro1951Ala
XM_011522380.1:c.6058C>G	XP_011520682.1:p.Pro2020Ala
XM_011522381.1:c.5359C>G	XP_011520683.1:p.Pro1787Ala
XM_005255124.4:c.6067C>G	XP_005255181.1:p.Pro2023Ala
XM_005255125.4:c.5695C>G	XP_005255182.1:p.Pro1899Ala
XM_006720848.3:c.5851C>G	XP_006720911.1:p.Pro1951Ala
XM_011522381.2:c.5359C>G	XP_011520683.1:p.Pro1787Ala
XM_017022944.1:c.6106C>G	XP_016878433.1:p.Pro2036Ala
NM_004380.3:c.6112C>G MANE Select	NP_004371.2:p.Pro2038Ala