Canonical Allele Identifier: CA2320568425
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714122A= , CM000681.2:g.6714122A= GRCh38
NC_000019.9:g.6714133A= , CM000681.1:g.6714133A= GRCh37
NC_000019.8:g.6665133A= NCBI36
NG_009557.1:g.11530T= , LRG_27:g.11530T=

Transcript Alleles

HGVS Amino-acid change
ENST00000695652.1:c.560-40T= ENSP00000512083.1:n.560-40T=
ENST00000245907.11:c.683-40T= MANE Select ENSP00000245907.4:n.683-40T=
ENST00000245907.10:c.683-40T= ENSP00000245907.4:n.683-40T=
ENST00000595577.1:n.187-40T=
NM_000064.3:c.683-40T= NP_000055.2:n.683-40T=
NM_000064.4:c.683-40T= MANE Select NP_000055.2:n.683-40T=