Canonical Allele Identifier: CA2320568564
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714411C= , CM000681.2:g.6714411C= GRCh38
NC_000019.9:g.6714422C= , CM000681.1:g.6714422C= GRCh37
NC_000019.8:g.6665422C= NCBI36
NG_009557.1:g.11241G= , LRG_27:g.11241G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.417G= ENSP00000512083.1:p.Leu139=
ENST00000245907.11:c.540G= MANE Select ENSP00000245907.4:p.Leu180=
ENST00000245907.10:c.540G= ENSP00000245907.4:p.Leu180=
NM_000064.3:c.540G= NP_000055.2:p.Leu180=
NM_000064.4:c.540G= MANE Select NP_000055.2:p.Leu180=