Canonical Allele Identifier: CA454908050

Gene: CCM2

Linked Data

• dbSNP Id: rs1258209042
• gnomAD v2: 7-45039959-G-A
• gnomAD v4: 7-45000360-G-A
• MyVariant Identifiers: chr7:g.45039959G>A (hg19) ; chr7:g.45000360G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.45000360G>A , CM000669.2:g.45000360G>A	GRCh38
NC_000007.13:g.45039959G>A , CM000669.1:g.45039959G>A	GRCh37
NC_000007.12:g.45006484G>A	NCBI36
NG_016295.1:g.5173G>A , LRG_664:g.5173G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258781.11:c.27G>A MANE Select	ENSP00000258781.7:p.Lys9=
ENST00000648329.1:c.27G>A	ENSP00000496916.1:p.Lys9=
ENST00000258781.10:c.27G>A	ENSP00000258781.6:p.Lys9=
ENST00000461377.5:n.383+503G>A
ENST00000478582.5:n.172G>A
ENST00000488727.5:c.27G>A	ENSP00000417251.1:p.Lys9=
ENST00000541586.5:c.27G>A	ENSP00000444725.1:p.Lys9=
ENST00000544363.5:c.27G>A	ENSP00000438035.1:p.Lys9=
NM_001167934.1:c.27G>A	NP_001161406.1:p.Lys9=
NM_001167935.1:c.27G>A	NP_001161407.1:p.Lys9=
NM_031443.3:c.27G>A , LRG_664t2:c.27G>A	NP_113631.1:p.Lys9=
NR_030770.1:n.112+503G>A
XM_011515562.1:c.27G>A	XP_011513864.1:p.Lys9=
XM_011515564.1:c.27G>A	XP_011513866.1:p.Lys9=
NM_001363458.1:c.27G>A	NP_001350387.1:p.Lys9=
NM_001363459.1:c.27G>A	NP_001350388.1:p.Lys9=
XM_017012673.1:c.27G>A	XP_016868162.1:p.Lys9=
NM_001363458.2:c.27G>A	NP_001350387.1:p.Lys9=
NM_001363459.2:c.27G>A	NP_001350388.1:p.Lys9=
NM_031443.4:c.27G>A MANE Select	NP_113631.1:p.Lys9=
NR_030770.2:n.112+503G>A
NM_001167934.2:c.27G>A	NP_001161406.1:p.Lys9=
NM_001167935.2:c.27G>A	NP_001161407.1:p.Lys9=