Canonical Allele Identifier: CA403632999
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6697457A>G , CM000681.2:g.6697457A>G GRCh38
NC_000019.9:g.6697468A>G , CM000681.1:g.6697468A>G GRCh37
NC_000019.8:g.6648468A>G NCBI36
NG_009557.1:g.28195T>C , LRG_27:g.28195T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000695651.1:n.1031T>C
ENST00000695652.1:c.2560T>C ENSP00000512083.1:p.Ser854Pro
ENST00000695653.1:c.592T>C ENSP00000512084.1:p.Ser198Pro
ENST00000695654.1:c.1807T>C ENSP00000512085.1:p.Ser603Pro
ENST00000695655.1:c.1624T>C ENSP00000512086.1:n.1624T>C
ENST00000695692.1:n.2047T>C
ENST00000245907.11:c.2683T>C MANE Select ENSP00000245907.4:p.Ser895Pro
ENST00000245907.10:c.2683T>C ENSP00000245907.4:p.Ser895Pro
ENST00000594005.1:n.259T>C
NM_000064.3:c.2683T>C NP_000055.2:p.Ser895Pro
NM_000064.4:c.2683T>C MANE Select NP_000055.2:p.Ser895Pro