Canonical Allele Identifier: CA2813436761

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697573G>T , CM000681.2:g.6697573G>T	GRCh38
NC_000019.9:g.6697584G>T , CM000681.1:g.6697584G>T	GRCh37
NC_000019.8:g.6648584G>T	NCBI36
NG_009557.1:g.28079C>A , LRG_27:g.28079C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.932-17C>A
ENST00000695652.1:c.2461-17C>A	ENSP00000512083.1:n.2461-17C>A
ENST00000695653.1:c.493-17C>A	ENSP00000512084.1:n.493-17C>A
ENST00000695654.1:c.1708-17C>A	ENSP00000512085.1:n.1708-17C>A
ENST00000695655.1:c.1525-17C>A	ENSP00000512086.1:n.1525-17C>A
ENST00000695692.1:n.1948-17C>A
ENST00000245907.11:c.2584-17C>A MANE Select	ENSP00000245907.4:n.2584-17C>A
ENST00000245907.10:c.2584-17C>A	ENSP00000245907.4:n.2584-17C>A
ENST00000594005.1:n.143C>A
NM_000064.3:c.2584-17C>A	NP_000055.2:n.2584-17C>A
NM_000064.4:c.2584-17C>A MANE Select	NP_000055.2:n.2584-17C>A