Canonical Allele Identifier: CA403642550
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713440C>A , CM000681.2:g.6713440C>A GRCh38
NC_000019.9:g.6713451C>A , CM000681.1:g.6713451C>A GRCh37
NC_000019.8:g.6664451C>A NCBI36
NG_009557.1:g.12212G>T , LRG_27:g.12212G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.720G>T ENSP00000512083.1:p.Arg240Ser
ENST00000695692.1:n.167G>T
ENST00000245907.11:c.843G>T MANE Select ENSP00000245907.4:p.Arg281Ser
ENST00000245907.10:c.843G>T ENSP00000245907.4:p.Arg281Ser
ENST00000595577.1:n.347G>T
ENST00000597442.5:n.93G>T
NM_000064.3:c.843G>T NP_000055.2:p.Arg281Ser
NM_000064.4:c.843G>T MANE Select NP_000055.2:p.Arg281Ser