Canonical Allele Identifier: CA403643233
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714228C>A , CM000681.2:g.6714228C>A GRCh38
NC_000019.9:g.6714239C>A , CM000681.1:g.6714239C>A GRCh37
NC_000019.8:g.6665239C>A NCBI36
NG_009557.1:g.11424G>T , LRG_27:g.11424G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.497G>T ENSP00000512083.1:p.Arg166Leu
ENST00000245907.11:c.620G>T MANE Select ENSP00000245907.4:p.Arg207Leu
ENST00000245907.10:c.620G>T ENSP00000245907.4:p.Arg207Leu
ENST00000595577.1:n.124G>T
NM_000064.3:c.620G>T NP_000055.2:p.Arg207Leu
NM_000064.4:c.620G>T MANE Select NP_000055.2:p.Arg207Leu