Canonical Allele Identifier: CA403642662
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713467G>C , CM000681.2:g.6713467G>C GRCh38
NC_000019.9:g.6713478G>C , CM000681.1:g.6713478G>C GRCh37
NC_000019.8:g.6664478G>C NCBI36
NG_009557.1:g.12185C>G , LRG_27:g.12185C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.693C>G ENSP00000512083.1:p.Ile231Met
ENST00000695692.1:n.140C>G
ENST00000245907.11:c.816C>G MANE Select ENSP00000245907.4:p.Ile272Met
ENST00000245907.10:c.816C>G ENSP00000245907.4:p.Ile272Met
ENST00000595577.1:n.320C>G
ENST00000597442.5:n.66C>G
NM_000064.3:c.816C>G NP_000055.2:p.Ile272Met
NM_000064.4:c.816C>G MANE Select NP_000055.2:p.Ile272Met