Canonical Allele Identifier: CA2320568413
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714110C= , CM000681.2:g.6714110C= GRCh38
NC_000019.9:g.6714121C= , CM000681.1:g.6714121C= GRCh37
NC_000019.8:g.6665121C= NCBI36
NG_009557.1:g.11542G= , LRG_27:g.11542G=

Transcript Alleles

HGVS Amino-acid change
ENST00000695652.1:c.560-28G= ENSP00000512083.1:n.560-28G=
ENST00000245907.11:c.683-28G= MANE Select ENSP00000245907.4:n.683-28G=
ENST00000245907.10:c.683-28G= ENSP00000245907.4:n.683-28G=
ENST00000595577.1:n.187-28G=
NM_000064.3:c.683-28G= NP_000055.2:n.683-28G=
NM_000064.4:c.683-28G= MANE Select NP_000055.2:n.683-28G=