Canonical Allele Identifier: CA2320559328
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs1967575946

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6698000dup , CM000681.2:g.6698000dup GRCh38
NC_000019.9:g.6698011dup , CM000681.1:g.6698011dup GRCh37
NC_000019.8:g.6649011dup NCBI36
NG_009557.1:g.27653dup , LRG_27:g.27653dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000695651.1:n.789-205dup
ENST00000695652.1:c.2318-205dup ENSP00000512083.1:n.2318-205dup
ENST00000695653.1:c.350-205dup ENSP00000512084.1:n.350-205dup
ENST00000695654.1:c.1565-205dup ENSP00000512085.1:n.1565-205dup
ENST00000695655.1:c.1382-205dup ENSP00000512086.1:n.1382-205dup
ENST00000695692.1:n.1805-205dup
ENST00000245907.11:c.2441-205dup MANE Select ENSP00000245907.4:n.2441-205dup
ENST00000245907.10:c.2441-205dup ENSP00000245907.4:n.2441-205dup
ENST00000602053.1:n.489-205dup
NM_000064.3:c.2441-205dup NP_000055.2:n.2441-205dup
NM_000064.4:c.2441-205dup MANE Select NP_000055.2:n.2441-205dup