Canonical Allele Identifier: CA2587878134

Gene: C3

Linked Data

• gnomAD v4: 19-6712774-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6712774T>A , CM000681.2:g.6712774T>A	GRCh38
NC_000019.9:g.6712785T>A , CM000681.1:g.6712785T>A	GRCh37
NC_000019.8:g.6663785T>A	NCBI36
NG_009557.1:g.12878A>T , LRG_27:g.12878A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.881-151A>T	ENSP00000512083.1:n.881-151A>T
ENST00000695654.1:c.128-151A>T	ENSP00000512085.1:n.128-151A>T
ENST00000695692.1:n.328-111A>T
ENST00000245907.11:c.1004-151A>T MANE Select	ENSP00000245907.4:n.1004-151A>T
ENST00000245907.10:c.1004-151A>T	ENSP00000245907.4:n.1004-151A>T
ENST00000594270.5:n.128-172A>T
ENST00000595577.1:n.508-151A>T
ENST00000597442.5:n.254-151A>T
NM_000064.3:c.1004-151A>T	NP_000055.2:n.1004-151A>T
NM_000064.4:c.1004-151A>T MANE Select	NP_000055.2:n.1004-151A>T