Canonical Allele Identifier: CA2320568419
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714116T= , CM000681.2:g.6714116T= GRCh38
NC_000019.9:g.6714127T= , CM000681.1:g.6714127T= GRCh37
NC_000019.8:g.6665127T= NCBI36
NG_009557.1:g.11536A= , LRG_27:g.11536A=

Transcript Alleles

HGVS Amino-acid change
ENST00000695652.1:c.560-34A= ENSP00000512083.1:n.560-34A=
ENST00000245907.11:c.683-34A= MANE Select ENSP00000245907.4:n.683-34A=
ENST00000245907.10:c.683-34A= ENSP00000245907.4:n.683-34A=
ENST00000595577.1:n.187-34A=
NM_000064.3:c.683-34A= NP_000055.2:n.683-34A=
NM_000064.4:c.683-34A= MANE Select NP_000055.2:n.683-34A=