Canonical Allele Identifier: CA2576592439

Gene: C3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6714117G>T , CM000681.2:g.6714117G>T	GRCh38
NC_000019.9:g.6714128G>T , CM000681.1:g.6714128G>T	GRCh37
NC_000019.8:g.6665128G>T	NCBI36
NG_009557.1:g.11535C>A , LRG_27:g.11535C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.560-35C>A	ENSP00000512083.1:n.560-35C>A
ENST00000245907.11:c.683-35C>A MANE Select	ENSP00000245907.4:n.683-35C>A
ENST00000245907.10:c.683-35C>A	ENSP00000245907.4:n.683-35C>A
ENST00000595577.1:n.187-35C>A
NM_000064.3:c.683-35C>A	NP_000055.2:n.683-35C>A
NM_000064.4:c.683-35C>A MANE Select	NP_000055.2:n.683-35C>A