Canonical Allele Identifier: CA2320568647
Gene: C3 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714598A= , CM000681.2:g.6714598A= GRCh38
NC_000019.9:g.6714609A= , CM000681.1:g.6714609A= GRCh37
NC_000019.8:g.6665609A= NCBI36
NG_009557.1:g.11054T= , LRG_27:g.11054T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.382-152T= ENSP00000512083.1:n.382-152T=
ENST00000245907.11:c.505-152T= MANE Select ENSP00000245907.4:n.505-152T=
ENST00000245907.10:c.505-152T= ENSP00000245907.4:n.505-152T=
NM_000064.3:c.505-152T= NP_000055.2:n.505-152T=
NM_000064.4:c.505-152T= MANE Select NP_000055.2:n.505-152T=
Search 100 bp 5'
Search 100 bp 3'