Canonical Allele Identifier: CA2673688569

Gene: C7

Linked Data

• gnomAD v4: 5-40964945-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.40964945C>A , CM000667.2:g.40964945C>A	GRCh38
NC_000005.9:g.40965047C>A , CM000667.1:g.40965047C>A	GRCh37
NC_000005.8:g.41000804C>A	NCBI36
NG_011692.1:g.60449C>A , LRG_30:g.60449C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486779.2:n.674+72C>A
ENST00000696333.1:c.1882+72C>A	ENSP00000512566.1:n.1882+72C>A
ENST00000696441.1:c.1882+72C>A	ENSP00000512631.1:n.1882+72C>A
ENST00000706664.1:n.1996+72C>A
ENST00000706666.1:n.1958+72C>A
ENST00000706667.1:n.2772+72C>A
ENST00000706668.1:n.2610+72C>A
ENST00000313164.10:c.1882+72C>A MANE Select	ENSP00000322061.9:n.1882+72C>A
ENST00000313164.9:c.1882+72C>A	ENSP00000322061.9:n.1882+72C>A
ENST00000486779.1:n.395+72C>A
NM_000587.2:c.1882+72C>A , LRG_30t1:c.1882+72C>A	NP_000578.2:n.1882+72C>A
XM_011514122.1:c.1882+72C>A	XP_011512424.1:n.1882+72C>A
NM_000587.3:c.1882+72C>A	NP_000578.2:n.1882+72C>A
NM_000587.4:c.1882+72C>A MANE Select	NP_000578.2:n.1882+72C>A