Canonical Allele Identifier: CA2320552874
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6685040T= , CM000681.2:g.6685040T= GRCh38
NC_000019.9:g.6685051T= , CM000681.1:g.6685051T= GRCh37
NC_000019.8:g.6636051T= NCBI36
NG_009557.1:g.40612A= , LRG_27:g.40612A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695651.1:n.2265A=
ENST00000695653.1:c.1826A= ENSP00000512084.1:p.Lys609=
ENST00000695654.1:c.2942A= ENSP00000512085.1:p.Lys981=
ENST00000695690.1:n.108A=
ENST00000695691.1:n.108A=
ENST00000245907.11:c.3917A= MANE Select ENSP00000245907.4:p.Lys1306=
ENST00000245907.10:c.3917A= ENSP00000245907.4:p.Lys1306=
ENST00000596238.1:n.360A=
ENST00000601008.1:c.241+1706A= ENSP00000471384.1:n.241+1706A=
NM_000064.3:c.3917A= NP_000055.2:p.Lys1306=
NM_000064.4:c.3917A= MANE Select NP_000055.2:p.Lys1306=