Canonical Allele Identifier: CA2320561798
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6701474C= , CM000681.2:g.6701474C= GRCh38
NC_000019.9:g.6701485C= , CM000681.1:g.6701485C= GRCh37
NC_000019.8:g.6652485C= NCBI36
NG_009557.1:g.24178G= , LRG_27:g.24178G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695651.1:n.788+653G=
ENST00000695652.1:c.2317+653G= ENSP00000512083.1:n.2317+653G=
ENST00000695653.1:c.349+653G= ENSP00000512084.1:n.349+653G=
ENST00000695654.1:c.1564+653G= ENSP00000512085.1:n.1564+653G=
ENST00000695655.1:c.1381+653G= ENSP00000512086.1:n.1381+653G=
ENST00000695692.1:n.1804+653G=
ENST00000245907.11:c.2440+653G= MANE Select ENSP00000245907.4:n.2440+653G=
ENST00000245907.10:c.2440+653G= ENSP00000245907.4:n.2440+653G=
ENST00000602053.1:n.488+653G=
NM_000064.3:c.2440+653G= NP_000055.2:n.2440+653G=
NM_000064.4:c.2440+653G= MANE Select NP_000055.2:n.2440+653G=