Canonical Allele Identifier: CA2576592405

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713568C>T , CM000681.2:g.6713568C>T	GRCh38
NC_000019.9:g.6713579C>T , CM000681.1:g.6713579C>T	GRCh37
NC_000019.8:g.6664579C>T	NCBI36
NG_009557.1:g.12084G>A , LRG_27:g.12084G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.651-59G>A	ENSP00000512083.1:n.651-59G>A
ENST00000695692.1:n.39G>A
ENST00000245907.11:c.774-59G>A MANE Select	ENSP00000245907.4:n.774-59G>A
ENST00000245907.10:c.774-59G>A	ENSP00000245907.4:n.774-59G>A
ENST00000595577.1:n.278-59G>A
ENST00000597442.5:n.24-59G>A
NM_000064.3:c.774-59G>A	NP_000055.2:n.774-59G>A
NM_000064.4:c.774-59G>A MANE Select	NP_000055.2:n.774-59G>A