Canonical Allele Identifier: CA403642922
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714014G>C , CM000681.2:g.6714014G>C GRCh38
NC_000019.9:g.6714025G>C , CM000681.1:g.6714025G>C GRCh37
NC_000019.8:g.6665025G>C NCBI36
NG_009557.1:g.11638C>G , LRG_27:g.11638C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.628C>G ENSP00000512083.1:p.Leu210Val
ENST00000245907.11:c.751C>G MANE Select ENSP00000245907.4:p.Leu251Val
ENST00000245907.10:c.751C>G ENSP00000245907.4:p.Leu251Val
ENST00000595577.1:n.255C>G
NM_000064.3:c.751C>G NP_000055.2:p.Leu251Val
NM_000064.4:c.751C>G MANE Select NP_000055.2:p.Leu251Val