Canonical Allele Identifier: CA2320559241
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6697825C= , CM000681.2:g.6697825C= GRCh38
NC_000019.9:g.6697836C= , CM000681.1:g.6697836C= GRCh37
NC_000019.8:g.6648836C= NCBI36
NG_009557.1:g.27827G= , LRG_27:g.27827G=

Transcript Alleles

HGVS Amino-acid change
ENST00000695651.1:n.789-31G=
ENST00000695652.1:c.2318-31G= ENSP00000512083.1:n.2318-31G=
ENST00000695653.1:c.350-31G= ENSP00000512084.1:n.350-31G=
ENST00000695654.1:c.1565-31G= ENSP00000512085.1:n.1565-31G=
ENST00000695655.1:c.1382-31G= ENSP00000512086.1:n.1382-31G=
ENST00000695692.1:n.1805-31G=
ENST00000245907.11:c.2441-31G= MANE Select ENSP00000245907.4:n.2441-31G=
ENST00000245907.10:c.2441-31G= ENSP00000245907.4:n.2441-31G=
ENST00000602053.1:n.489-31G=
NM_000064.3:c.2441-31G= NP_000055.2:n.2441-31G=
NM_000064.4:c.2441-31G= MANE Select NP_000055.2:n.2441-31G=