Canonical Allele Identifier: CA2320568468
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714217C= , CM000681.2:g.6714217C= GRCh38
NC_000019.9:g.6714228C= , CM000681.1:g.6714228C= GRCh37
NC_000019.8:g.6665228C= NCBI36
NG_009557.1:g.11435G= , LRG_27:g.11435G=

Transcript Alleles

HGVS Amino-acid change
ENST00000695652.1:c.508G= ENSP00000512083.1:p.Glu170=
ENST00000245907.11:c.631G= MANE Select ENSP00000245907.4:p.Glu211=
ENST00000245907.10:c.631G= ENSP00000245907.4:p.Glu211=
ENST00000595577.1:n.135G=
NM_000064.3:c.631G= NP_000055.2:p.Glu211=
NM_000064.4:c.631G= MANE Select NP_000055.2:p.Glu211=