Canonical Allele Identifier: CA403642178
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713254T>C , CM000681.2:g.6713254T>C GRCh38
NC_000019.9:g.6713265T>C , CM000681.1:g.6713265T>C GRCh37
NC_000019.8:g.6664265T>C NCBI36
NG_009557.1:g.12398A>G , LRG_27:g.12398A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000695652.1:c.815A>G ENSP00000512083.1:p.Asn272Ser
ENST00000695654.1:c.62A>G ENSP00000512085.1:p.Asn21Ser
ENST00000695692.1:n.262A>G
ENST00000245907.11:c.938A>G MANE Select ENSP00000245907.4:p.Asn313Ser
ENST00000245907.10:c.938A>G ENSP00000245907.4:p.Asn313Ser
ENST00000594270.5:n.62A>G
ENST00000595577.1:n.442A>G
ENST00000597442.5:n.188A>G
NM_000064.3:c.938A>G NP_000055.2:p.Asn313Ser
NM_000064.4:c.938A>G MANE Select NP_000055.2:p.Asn313Ser