Canonical Allele Identifier: CA2320567843
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713259C= , CM000681.2:g.6713259C= GRCh38
NC_000019.9:g.6713270C= , CM000681.1:g.6713270C= GRCh37
NC_000019.8:g.6664270C= NCBI36
NG_009557.1:g.12393G= , LRG_27:g.12393G=

Transcript Alleles

HGVS Amino-acid change
ENST00000695652.1:c.810G= ENSP00000512083.1:p.Val270=
ENST00000695654.1:c.57G= ENSP00000512085.1:p.Val19=
ENST00000695692.1:n.257G=
ENST00000245907.11:c.933G= MANE Select ENSP00000245907.4:p.Val311=
ENST00000245907.10:c.933G= ENSP00000245907.4:p.Val311=
ENST00000594270.5:n.57G=
ENST00000595577.1:n.437G=
ENST00000597442.5:n.183G=
NM_000064.3:c.933G= NP_000055.2:p.Val311=
NM_000064.4:c.933G= MANE Select NP_000055.2:p.Val311=