Canonical Allele Identifier: CA2320550407
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6679405A= , CM000681.2:g.6679405A= GRCh38
NC_000019.9:g.6679416A= , CM000681.1:g.6679416A= GRCh37
NC_000019.8:g.6630416A= NCBI36
NG_009557.1:g.46247T= , LRG_27:g.46247T=

Transcript Alleles

HGVS Amino-acid change
ENST00000695651.1:n.2894+2T=
ENST00000695653.1:c.2455+2T= ENSP00000512084.1:n.2455+2T=
ENST00000695654.1:c.3571+2T= ENSP00000512085.1:n.3571+2T=
ENST00000695689.1:c.517+2T= ENSP00000512101.1:n.517+2T=
ENST00000695690.1:n.1611+2T=
ENST00000695691.1:n.1407+2T=
ENST00000245907.11:c.4546+2T= MANE Select ENSP00000245907.4:n.4546+2T=
ENST00000245907.10:c.4546+2T= ENSP00000245907.4:n.4546+2T=
ENST00000599668.1:n.143T=
ENST00000599899.5:n.1505+2T=
ENST00000601008.1:c.242-1447T= ENSP00000471384.1:n.242-1447T=
NM_000064.3:c.4546+2T= NP_000055.2:n.4546+2T=
NM_000064.4:c.4546+2T= MANE Select NP_000055.2:n.4546+2T=