Canonical Allele Identifier: CA403642798
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713501T>C , CM000681.2:g.6713501T>C GRCh38
NC_000019.9:g.6713512T>C , CM000681.1:g.6713512T>C GRCh37
NC_000019.8:g.6664512T>C NCBI36
NG_009557.1:g.12151A>G , LRG_27:g.12151A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.659A>G ENSP00000512083.1:p.Tyr220Cys
ENST00000695692.1:n.106A>G
ENST00000245907.11:c.782A>G MANE Select ENSP00000245907.4:p.Tyr261Cys
ENST00000245907.10:c.782A>G ENSP00000245907.4:p.Tyr261Cys
ENST00000595577.1:n.286A>G
ENST00000597442.5:n.32A>G
NM_000064.3:c.782A>G NP_000055.2:p.Tyr261Cys
NM_000064.4:c.782A>G MANE Select NP_000055.2:p.Tyr261Cys