Canonical Allele Identifier: CA403633975
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6697723A>C , CM000681.2:g.6697723A>C GRCh38
NC_000019.9:g.6697734A>C , CM000681.1:g.6697734A>C GRCh37
NC_000019.8:g.6648734A>C NCBI36
NG_009557.1:g.27929T>G , LRG_27:g.27929T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000695651.1:n.860T>G
ENST00000695652.1:c.2389T>G ENSP00000512083.1:p.Ser797Ala
ENST00000695653.1:c.421T>G ENSP00000512084.1:p.Ser141Ala
ENST00000695654.1:c.1636T>G ENSP00000512085.1:p.Ser546Ala
ENST00000695655.1:c.1453T>G ENSP00000512086.1:n.1453T>G
ENST00000695692.1:n.1876T>G
ENST00000245907.11:c.2512T>G MANE Select ENSP00000245907.4:p.Ser838Ala
ENST00000245907.10:c.2512T>G ENSP00000245907.4:p.Ser838Ala
ENST00000602053.1:n.560T>G
NM_000064.3:c.2512T>G NP_000055.2:p.Ser838Ala
NM_000064.4:c.2512T>G MANE Select NP_000055.2:p.Ser838Ala