Canonical Allele Identifier: CA631657443
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs1568217815

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6698012_6698024del , CM000681.2:g.6698012_6698024del GRCh38
NC_000019.9:g.6698023_6698035del , CM000681.1:g.6698023_6698035del GRCh37
NC_000019.8:g.6649023_6649035del NCBI36
NG_009557.1:g.27629_27641del , LRG_27:g.27629_27641del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695651.1:n.789-229_789-217del
ENST00000695652.1:c.2318-229_2318-217del ENSP00000512083.1:n.2318-229_2318-217del
ENST00000695653.1:c.350-229_350-217del ENSP00000512084.1:n.350-229_350-217del
ENST00000695654.1:c.1565-229_1565-217del ENSP00000512085.1:n.1565-229_1565-217del
ENST00000695655.1:c.1382-229_1382-217del ENSP00000512086.1:n.1382-229_1382-217del
ENST00000695692.1:n.1805-229_1805-217del
ENST00000245907.11:c.2441-229_2441-217del MANE Select ENSP00000245907.4:n.2441-229_2441-217del
ENST00000245907.10:c.2441-229_2441-217del ENSP00000245907.4:n.2441-229_2441-217del
ENST00000602053.1:n.489-229_489-217del
NM_000064.3:c.2441-229_2441-217del NP_000055.2:n.2441-229_2441-217del
NM_000064.4:c.2441-229_2441-217del MANE Select NP_000055.2:n.2441-229_2441-217del