Canonical Allele Identifier: CA2682672885

Gene: CCM2

Linked Data

• gnomAD v4: 7-45000371-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.45000371T>C , CM000669.2:g.45000371T>C	GRCh38
NC_000007.13:g.45039970T>C , CM000669.1:g.45039970T>C	GRCh37
NC_000007.12:g.45006495T>C	NCBI36
NG_016295.1:g.5184T>C , LRG_664:g.5184T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000258781.11:c.30+8T>C MANE Select	ENSP00000258781.7:n.30+8T>C
ENST00000648329.1:c.30+8T>C	ENSP00000496916.1:n.30+8T>C
ENST00000258781.10:c.30+8T>C	ENSP00000258781.6:n.30+8T>C
ENST00000461377.5:n.383+514T>C
ENST00000478582.5:n.175+8T>C
ENST00000488727.5:c.30+8T>C	ENSP00000417251.1:n.30+8T>C
ENST00000541586.5:c.30+8T>C	ENSP00000444725.1:n.30+8T>C
ENST00000544363.5:c.30+8T>C	ENSP00000438035.1:n.30+8T>C
NM_001167934.1:c.30+8T>C	NP_001161406.1:n.30+8T>C
NM_001167935.1:c.30+8T>C	NP_001161407.1:n.30+8T>C
NM_031443.3:c.30+8T>C , LRG_664t2:c.30+8T>C	NP_113631.1:n.30+8T>C
NR_030770.1:n.112+514T>C
XM_011515562.1:c.30+8T>C	XP_011513864.1:n.30+8T>C
XM_011515564.1:c.30+8T>C	XP_011513866.1:n.30+8T>C
NM_001363458.1:c.30+8T>C	NP_001350387.1:n.30+8T>C
NM_001363459.1:c.30+8T>C	NP_001350388.1:n.30+8T>C
XM_017012673.1:c.30+8T>C	XP_016868162.1:n.30+8T>C
NM_001363458.2:c.30+8T>C	NP_001350387.1:n.30+8T>C
NM_001363459.2:c.30+8T>C	NP_001350388.1:n.30+8T>C
NM_031443.4:c.30+8T>C MANE Select	NP_113631.1:n.30+8T>C
NR_030770.2:n.112+514T>C
NM_001167934.2:c.30+8T>C	NP_001161406.1:n.30+8T>C
NM_001167935.2:c.30+8T>C	NP_001161407.1:n.30+8T>C