Canonical Allele Identifier: CA2839183306

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6714109C>T , CM000681.2:g.6714109C>T	GRCh38
NC_000019.9:g.6714120C>T , CM000681.1:g.6714120C>T	GRCh37
NC_000019.8:g.6665120C>T	NCBI36
NG_009557.1:g.11543G>A , LRG_27:g.11543G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.560-27G>A	ENSP00000512083.1:n.560-27G>A
ENST00000245907.11:c.683-27G>A MANE Select	ENSP00000245907.4:n.683-27G>A
ENST00000245907.10:c.683-27G>A	ENSP00000245907.4:n.683-27G>A
ENST00000595577.1:n.187-27G>A
NM_000064.3:c.683-27G>A	NP_000055.2:n.683-27G>A
NM_000064.4:c.683-27G>A MANE Select	NP_000055.2:n.683-27G>A