Canonical Allele Identifier: CA2587878130

Gene: C3

Linked Data

• gnomAD v4: 19-6712773-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6712773C>A , CM000681.2:g.6712773C>A	GRCh38
NC_000019.9:g.6712784C>A , CM000681.1:g.6712784C>A	GRCh37
NC_000019.8:g.6663784C>A	NCBI36
NG_009557.1:g.12879G>T , LRG_27:g.12879G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.881-150G>T	ENSP00000512083.1:n.881-150G>T
ENST00000695654.1:c.128-150G>T	ENSP00000512085.1:n.128-150G>T
ENST00000695692.1:n.328-110G>T
ENST00000245907.11:c.1004-150G>T MANE Select	ENSP00000245907.4:n.1004-150G>T
ENST00000245907.10:c.1004-150G>T	ENSP00000245907.4:n.1004-150G>T
ENST00000594270.5:n.128-171G>T
ENST00000595577.1:n.508-150G>T
ENST00000597442.5:n.254-150G>T
NM_000064.3:c.1004-150G>T	NP_000055.2:n.1004-150G>T
NM_000064.4:c.1004-150G>T MANE Select	NP_000055.2:n.1004-150G>T