Canonical Allele Identifier: CA2320551902
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6682858T= , CM000681.2:g.6682858T= GRCh38
NC_000019.9:g.6682869T= , CM000681.1:g.6682869T= GRCh37
NC_000019.8:g.6633869T= NCBI36
NG_009557.1:g.42794A= , LRG_27:g.42794A=

Transcript Alleles

HGVS Amino-acid change
ENST00000695651.1:n.2521-629A=
ENST00000695653.1:c.2082-629A= ENSP00000512084.1:n.2082-629A=
ENST00000695654.1:c.3198-629A= ENSP00000512085.1:n.3198-629A=
ENST00000695689.1:c.84-192A= ENSP00000512101.1:n.84-192A=
ENST00000695690.1:n.364-629A=
ENST00000695691.1:n.364-629A=
ENST00000245907.11:c.4173-629A= MANE Select ENSP00000245907.4:n.4173-629A=
ENST00000245907.10:c.4173-629A= ENSP00000245907.4:n.4173-629A=
ENST00000596548.1:c.294-629A= ENSP00000469744.1:n.294-629A=
ENST00000599899.5:n.503A=
ENST00000601008.1:c.241+3888A= ENSP00000471384.1:n.241+3888A=
NM_000064.3:c.4173-629A= NP_000055.2:n.4173-629A=
NM_000064.4:c.4173-629A= MANE Select NP_000055.2:n.4173-629A=