Canonical Allele Identifier: CA2320566749
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6710848G= , CM000681.2:g.6710848G= GRCh38
NC_000019.9:g.6710859G= , CM000681.1:g.6710859G= GRCh37
NC_000019.8:g.6661859G= NCBI36
NG_009557.1:g.14804C= , LRG_27:g.14804C=

Transcript Alleles

HGVS Amino-acid change
ENST00000695652.1:c.1357-3C= ENSP00000512083.1:n.1357-3C=
ENST00000695654.1:c.604-3C= ENSP00000512085.1:n.604-3C=
ENST00000695655.1:c.382C= ENSP00000512086.1:p.Gln128=
ENST00000695692.1:n.844-3C=
ENST00000245907.11:c.1480-3C= MANE Select ENSP00000245907.4:n.1480-3C=
ENST00000245907.10:c.1480-3C= ENSP00000245907.4:n.1480-3C=
ENST00000600763.1:n.110C=
NM_000064.3:c.1480-3C= NP_000055.2:n.1480-3C=
NM_000064.4:c.1480-3C= MANE Select NP_000055.2:n.1480-3C=