Canonical Allele Identifier: CA403643198
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714211A>C , CM000681.2:g.6714211A>C GRCh38
NC_000019.9:g.6714222A>C , CM000681.1:g.6714222A>C GRCh37
NC_000019.8:g.6665222A>C NCBI36
NG_009557.1:g.11441T>G , LRG_27:g.11441T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000695652.1:c.514T>G ENSP00000512083.1:p.Ser172Ala
ENST00000245907.11:c.637T>G MANE Select ENSP00000245907.4:p.Ser213Ala
ENST00000245907.10:c.637T>G ENSP00000245907.4:p.Ser213Ala
ENST00000595577.1:n.141T>G
NM_000064.3:c.637T>G NP_000055.2:p.Ser213Ala
NM_000064.4:c.637T>G MANE Select NP_000055.2:p.Ser213Ala