Canonical Allele Identifier: CA403633969
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6697720C>A , CM000681.2:g.6697720C>A GRCh38
NC_000019.9:g.6697731C>A , CM000681.1:g.6697731C>A GRCh37
NC_000019.8:g.6648731C>A NCBI36
NG_009557.1:g.27932G>T , LRG_27:g.27932G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000695651.1:n.863G>T
ENST00000695652.1:c.2392G>T ENSP00000512083.1:p.Val798Phe
ENST00000695653.1:c.424G>T ENSP00000512084.1:p.Val142Phe
ENST00000695654.1:c.1639G>T ENSP00000512085.1:p.Val547Phe
ENST00000695655.1:c.1456G>T ENSP00000512086.1:n.1456G>T
ENST00000695692.1:n.1879G>T
ENST00000245907.11:c.2515G>T MANE Select ENSP00000245907.4:p.Val839Phe
ENST00000245907.10:c.2515G>T ENSP00000245907.4:p.Val839Phe
ENST00000602053.1:n.563G>T
NM_000064.3:c.2515G>T NP_000055.2:p.Val839Phe
NM_000064.4:c.2515G>T MANE Select NP_000055.2:p.Val839Phe