Canonical Allele Identifier: CA403642235
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713275A>T , CM000681.2:g.6713275A>T GRCh38
NC_000019.9:g.6713286A>T , CM000681.1:g.6713286A>T GRCh37
NC_000019.8:g.6664286A>T NCBI36
NG_009557.1:g.12377T>A , LRG_27:g.12377T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.794T>A ENSP00000512083.1:p.Val265Glu
ENST00000695654.1:c.41T>A ENSP00000512085.1:p.Val14Glu
ENST00000695692.1:n.241T>A
ENST00000245907.11:c.917T>A MANE Select ENSP00000245907.4:p.Val306Glu
ENST00000245907.10:c.917T>A ENSP00000245907.4:p.Val306Glu
ENST00000594270.5:n.41T>A
ENST00000595577.1:n.421T>A
ENST00000597442.5:n.167T>A
NM_000064.3:c.917T>A NP_000055.2:p.Val306Glu
NM_000064.4:c.917T>A MANE Select NP_000055.2:p.Val306Glu