Canonical Allele Identifier: CA2320568571
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714429C= , CM000681.2:g.6714429C= GRCh38
NC_000019.9:g.6714440C= , CM000681.1:g.6714440C= GRCh37
NC_000019.8:g.6665440C= NCBI36
NG_009557.1:g.11223G= , LRG_27:g.11223G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.399G= ENSP00000512083.1:p.Pro133=
ENST00000245907.11:c.522G= MANE Select ENSP00000245907.4:p.Pro174=
ENST00000245907.10:c.522G= ENSP00000245907.4:p.Pro174=
NM_000064.3:c.522G= NP_000055.2:p.Pro174=
NM_000064.4:c.522G= MANE Select NP_000055.2:p.Pro174=