Canonical Allele Identifier: CA2320568469
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714218A= , CM000681.2:g.6714218A= GRCh38
NC_000019.9:g.6714229A= , CM000681.1:g.6714229A= GRCh37
NC_000019.8:g.6665229A= NCBI36
NG_009557.1:g.11434T= , LRG_27:g.11434T=

Transcript Alleles

HGVS Amino-acid change
ENST00000695652.1:c.507T= ENSP00000512083.1:p.Tyr169=
ENST00000245907.11:c.630T= MANE Select ENSP00000245907.4:p.Tyr210=
ENST00000245907.10:c.630T= ENSP00000245907.4:p.Tyr210=
ENST00000595577.1:n.134T=
NM_000064.3:c.630T= NP_000055.2:p.Tyr210=
NM_000064.4:c.630T= MANE Select NP_000055.2:p.Tyr210=