Canonical Allele Identifier: CA2320551905
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6682862G= , CM000681.2:g.6682862G= GRCh38
NC_000019.9:g.6682873G= , CM000681.1:g.6682873G= GRCh37
NC_000019.8:g.6633873G= NCBI36
NG_009557.1:g.42790C= , LRG_27:g.42790C=

Transcript Alleles

HGVS Amino-acid change
ENST00000695651.1:n.2521-633C=
ENST00000695653.1:c.2082-633C= ENSP00000512084.1:n.2082-633C=
ENST00000695654.1:c.3198-633C= ENSP00000512085.1:n.3198-633C=
ENST00000695689.1:c.84-196C= ENSP00000512101.1:n.84-196C=
ENST00000695690.1:n.364-633C=
ENST00000695691.1:n.364-633C=
ENST00000245907.11:c.4173-633C= MANE Select ENSP00000245907.4:n.4173-633C=
ENST00000245907.10:c.4173-633C= ENSP00000245907.4:n.4173-633C=
ENST00000596548.1:c.294-633C= ENSP00000469744.1:n.294-633C=
ENST00000599899.5:n.499C=
ENST00000601008.1:c.241+3884C= ENSP00000471384.1:n.241+3884C=
NM_000064.3:c.4173-633C= NP_000055.2:n.4173-633C=
NM_000064.4:c.4173-633C= MANE Select NP_000055.2:n.4173-633C=