Canonical Allele Identifier: CA2320551913
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6682905A= , CM000681.2:g.6682905A= GRCh38
NC_000019.9:g.6682916A= , CM000681.1:g.6682916A= GRCh37
NC_000019.8:g.6633916A= NCBI36
NG_009557.1:g.42747T= , LRG_27:g.42747T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695651.1:n.2521-676T=
ENST00000695653.1:c.2082-676T= ENSP00000512084.1:n.2082-676T=
ENST00000695654.1:c.3198-676T= ENSP00000512085.1:n.3198-676T=
ENST00000695689.1:c.84-239T= ENSP00000512101.1:n.84-239T=
ENST00000695690.1:n.364-676T=
ENST00000695691.1:n.364-676T=
ENST00000245907.11:c.4173-676T= MANE Select ENSP00000245907.4:n.4173-676T=
ENST00000245907.10:c.4173-676T= ENSP00000245907.4:n.4173-676T=
ENST00000596548.1:c.294-676T= ENSP00000469744.1:n.294-676T=
ENST00000599899.5:n.456T=
ENST00000601008.1:c.241+3841T= ENSP00000471384.1:n.241+3841T=
NM_000064.3:c.4173-676T= NP_000055.2:n.4173-676T=
NM_000064.4:c.4173-676T= MANE Select NP_000055.2:n.4173-676T=