Canonical Allele Identifier: CA1704061518

Gene: CCM2

Linked Data

• dbSNP Id: rs1798658070

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.45064236A>G , CM000669.2:g.45064236A>G	GRCh38
NC_000007.13:g.45103835A>G , CM000669.1:g.45103835A>G	GRCh37
NC_000007.12:g.45070360A>G	NCBI36
NG_016295.1:g.69049A>G , LRG_664:g.69049A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258781.11:c.289-227A>G MANE Select	ENSP00000258781.7:n.289-227A>G
ENST00000648329.1:c.289-227A>G	ENSP00000496916.1:n.289-227A>G
ENST00000258781.10:c.289-227A>G	ENSP00000258781.6:n.289-227A>G
ENST00000381112.7:c.352-227A>G	ENSP00000370503.3:n.352-227A>G
ENST00000461377.5:n.642-227A>G
ENST00000472223.5:n.356-227A>G
ENST00000474617.1:c.271-227A>G	ENSP00000419474.1:n.271-227A>G
ENST00000475551.5:c.271-227A>G	ENSP00000417180.1:n.271-227A>G
ENST00000476594.1:n.374-227A>G
ENST00000478169.5:n.511-227A>G
ENST00000478582.5:n.500-227A>G
ENST00000480658.5:n.301-4207A>G
ENST00000482714.5:n.211-227A>G
ENST00000488727.5:c.289-227A>G	ENSP00000417251.1:n.289-227A>G
ENST00000492883.5:n.301-227A>G
ENST00000541586.5:c.115-227A>G	ENSP00000444725.1:n.115-227A>G
ENST00000544363.5:c.289-227A>G	ENSP00000438035.1:n.289-227A>G
NM_001029835.2:c.352-227A>G , LRG_664t1:c.352-227A>G	NP_001025006.1:n.352-227A>G
NM_001167934.1:c.115-227A>G	NP_001161406.1:n.115-227A>G
NM_001167935.1:c.289-227A>G	NP_001161407.1:n.289-227A>G
NM_031443.3:c.289-227A>G , LRG_664t2:c.289-227A>G	NP_113631.1:n.289-227A>G
NR_030770.1:n.371-227A>G
XM_006715785.2:c.178-227A>G	XP_006715848.1:n.178-227A>G
XM_006715786.2:c.352-227A>G	XP_006715849.1:n.352-227A>G
XM_011515561.1:c.352-227A>G	XP_011513863.1:n.352-227A>G
XM_011515562.1:c.289-227A>G	XP_011513864.1:n.289-227A>G
XM_011515563.1:c.178-227A>G	XP_011513865.1:n.178-227A>G
XM_011515564.1:c.115-227A>G	XP_011513866.1:n.115-227A>G
XR_428088.2:n.365-227A>G
NM_001363458.1:c.289-227A>G	NP_001350387.1:n.289-227A>G
NM_001363459.1:c.115-227A>G	NP_001350388.1:n.115-227A>G
XM_006715785.4:c.178-227A>G	XP_006715848.1:n.178-227A>G
XM_006715786.3:c.352-227A>G	XP_006715849.1:n.352-227A>G
XM_011515561.2:c.352-227A>G	XP_011513863.1:n.352-227A>G
XM_011515563.3:c.178-227A>G	XP_011513865.1:n.178-227A>G
XM_017012671.1:c.352-227A>G	XP_016868160.1:n.352-227A>G
XM_017012672.2:c.178-227A>G	XP_016868161.1:n.178-227A>G
XM_017012673.1:c.115-227A>G	XP_016868162.1:n.115-227A>G
XR_428088.3:n.385-227A>G
NM_001363458.2:c.289-227A>G	NP_001350387.1:n.289-227A>G
NM_001363459.2:c.115-227A>G	NP_001350388.1:n.115-227A>G
NM_031443.4:c.289-227A>G MANE Select	NP_113631.1:n.289-227A>G
NR_030770.2:n.371-227A>G
NM_001167934.2:c.115-227A>G	NP_001161406.1:n.115-227A>G
NM_001167935.2:c.289-227A>G	NP_001161407.1:n.289-227A>G