Canonical Allele Identifier: CA403642947
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714025T>C , CM000681.2:g.6714025T>C GRCh38
NC_000019.9:g.6714036T>C , CM000681.1:g.6714036T>C GRCh37
NC_000019.8:g.6665036T>C NCBI36
NG_009557.1:g.11627A>G , LRG_27:g.11627A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.617A>G ENSP00000512083.1:p.Asn206Ser
ENST00000245907.11:c.740A>G MANE Select ENSP00000245907.4:p.Asn247Ser
ENST00000245907.10:c.740A>G ENSP00000245907.4:p.Asn247Ser
ENST00000595577.1:n.244A>G
NM_000064.3:c.740A>G NP_000055.2:p.Asn247Ser
NM_000064.4:c.740A>G MANE Select NP_000055.2:p.Asn247Ser