Canonical Allele Identifier: CA403642331
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs753979097
gnomAD v4: 19-6713302-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713302G>T , CM000681.2:g.6713302G>T GRCh38
NC_000019.9:g.6713313G>T , CM000681.1:g.6713313G>T GRCh37
NC_000019.8:g.6664313G>T NCBI36
NG_009557.1:g.12350C>A , LRG_27:g.12350C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.767C>A ENSP00000512083.1:p.Ser256Ter
ENST00000695654.1:c.14C>A ENSP00000512085.1:p.Ser5Ter
ENST00000695692.1:n.214C>A
ENST00000245907.11:c.890C>A MANE Select ENSP00000245907.4:p.Ser297Ter
ENST00000245907.10:c.890C>A ENSP00000245907.4:p.Ser297Ter
ENST00000594270.5:n.14C>A
ENST00000595577.1:n.394C>A
ENST00000597442.5:n.140C>A
NM_000064.3:c.890C>A NP_000055.2:p.Ser297Ter
NM_000064.4:c.890C>A MANE Select NP_000055.2:p.Ser297Ter