Canonical Allele Identifier: CA2813446681

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6712928G>C , CM000681.2:g.6712928G>C	GRCh38
NC_000019.9:g.6712939G>C , CM000681.1:g.6712939G>C	GRCh37
NC_000019.8:g.6663939G>C	NCBI36
NG_009557.1:g.12724C>G , LRG_27:g.12724C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.880+261C>G	ENSP00000512083.1:n.880+261C>G
ENST00000695654.1:c.127+261C>G	ENSP00000512085.1:n.127+261C>G
ENST00000695692.1:n.327+261C>G
ENST00000245907.11:c.1003+261C>G MANE Select	ENSP00000245907.4:n.1003+261C>G
ENST00000245907.10:c.1003+261C>G	ENSP00000245907.4:n.1003+261C>G
ENST00000594270.5:n.127+261C>G
ENST00000595577.1:n.507+261C>G
ENST00000597442.5:n.253+261C>G
NM_000064.3:c.1003+261C>G	NP_000055.2:n.1003+261C>G
NM_000064.4:c.1003+261C>G MANE Select	NP_000055.2:n.1003+261C>G