Canonical Allele Identifier: CA403642171
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713251G>T , CM000681.2:g.6713251G>T GRCh38
NC_000019.9:g.6713262G>T , CM000681.1:g.6713262G>T GRCh37
NC_000019.8:g.6664262G>T NCBI36
NG_009557.1:g.12401C>A , LRG_27:g.12401C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000695652.1:c.818C>A ENSP00000512083.1:p.Pro273His
ENST00000695654.1:c.65C>A ENSP00000512085.1:p.Pro22His
ENST00000695692.1:n.265C>A
ENST00000245907.11:c.941C>A MANE Select ENSP00000245907.4:p.Pro314His
ENST00000245907.10:c.941C>A ENSP00000245907.4:p.Pro314His
ENST00000594270.5:n.65C>A
ENST00000595577.1:n.445C>A
ENST00000597442.5:n.191C>A
NM_000064.3:c.941C>A NP_000055.2:p.Pro314His
NM_000064.4:c.941C>A MANE Select NP_000055.2:p.Pro314His