Canonical Allele Identifier: CA2673689388

Gene: C7

Linked Data

• gnomAD v4: 5-40979666-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.40979666C>A , CM000667.2:g.40979666C>A	GRCh38
NC_000005.9:g.40979768C>A , CM000667.1:g.40979768C>A	GRCh37
NC_000005.8:g.41015525C>A	NCBI36
NG_011692.1:g.75170C>A , LRG_30:g.75170C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696333.1:c.2166-59C>A	ENSP00000512566.1:n.2166-59C>A
ENST00000696441.1:c.2166-59C>A	ENSP00000512631.1:n.2166-59C>A
ENST00000696442.1:n.100-59C>A
ENST00000706664.1:n.2280-59C>A
ENST00000706666.1:n.2241+2826C>A
ENST00000706667.1:n.3056-59C>A
ENST00000706668.1:n.2894-59C>A
ENST00000313164.10:c.2166-59C>A MANE Select	ENSP00000322061.9:n.2166-59C>A
ENST00000313164.9:c.2166-59C>A	ENSP00000322061.9:n.2166-59C>A
ENST00000464864.1:n.179-59C>A
ENST00000494960.5:n.166-59C>A
NM_000587.2:c.2166-59C>A , LRG_30t1:c.2166-59C>A	NP_000578.2:n.2166-59C>A
XM_011514122.1:c.2166-59C>A	XP_011512424.1:n.2166-59C>A
NM_000587.3:c.2166-59C>A	NP_000578.2:n.2166-59C>A
NM_000587.4:c.2166-59C>A MANE Select	NP_000578.2:n.2166-59C>A