Canonical Allele Identifier: CA2320559200
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6697729G= , CM000681.2:g.6697729G= GRCh38
NC_000019.9:g.6697740G= , CM000681.1:g.6697740G= GRCh37
NC_000019.8:g.6648740G= NCBI36
NG_009557.1:g.27923C= , LRG_27:g.27923C=

Transcript Alleles

HGVS Amino-acid change
ENST00000695651.1:n.854C=
ENST00000695652.1:c.2383C= ENSP00000512083.1:p.Pro795=
ENST00000695653.1:c.415C= ENSP00000512084.1:p.Pro139=
ENST00000695654.1:c.1630C= ENSP00000512085.1:p.Pro544=
ENST00000695655.1:c.1447C= ENSP00000512086.1:n.1447C=
ENST00000695692.1:n.1870C=
ENST00000245907.11:c.2506C= MANE Select ENSP00000245907.4:p.Pro836=
ENST00000245907.10:c.2506C= ENSP00000245907.4:p.Pro836=
ENST00000602053.1:n.554C=
NM_000064.3:c.2506C= NP_000055.2:p.Pro836=
NM_000064.4:c.2506C= MANE Select NP_000055.2:p.Pro836=