Canonical Allele Identifier: CA2673689385

Gene: C7

Linked Data

• gnomAD v4: 5-40979664-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.40979664C>G , CM000667.2:g.40979664C>G	GRCh38
NC_000005.9:g.40979766C>G , CM000667.1:g.40979766C>G	GRCh37
NC_000005.8:g.41015523C>G	NCBI36
NG_011692.1:g.75168C>G , LRG_30:g.75168C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696333.1:c.2166-61C>G	ENSP00000512566.1:n.2166-61C>G
ENST00000696441.1:c.2166-61C>G	ENSP00000512631.1:n.2166-61C>G
ENST00000696442.1:n.100-61C>G
ENST00000706664.1:n.2280-61C>G
ENST00000706666.1:n.2241+2824C>G
ENST00000706667.1:n.3056-61C>G
ENST00000706668.1:n.2894-61C>G
ENST00000313164.10:c.2166-61C>G MANE Select	ENSP00000322061.9:n.2166-61C>G
ENST00000313164.9:c.2166-61C>G	ENSP00000322061.9:n.2166-61C>G
ENST00000464864.1:n.179-61C>G
ENST00000494960.5:n.166-61C>G
NM_000587.2:c.2166-61C>G , LRG_30t1:c.2166-61C>G	NP_000578.2:n.2166-61C>G
XM_011514122.1:c.2166-61C>G	XP_011512424.1:n.2166-61C>G
NM_000587.3:c.2166-61C>G	NP_000578.2:n.2166-61C>G
NM_000587.4:c.2166-61C>G MANE Select	NP_000578.2:n.2166-61C>G