Canonical Allele Identifier: CA2587871867
Gene: C3 HGNC NCBI

Linked Data

gnomAD v4: 19-6679507-ATG-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6679510_6679511del , CM000681.2:g.6679510_6679511del GRCh38
NC_000019.9:g.6679521_6679522del , CM000681.1:g.6679521_6679522del GRCh37
NC_000019.8:g.6630521_6630522del NCBI36
NG_009557.1:g.46143_46144del , LRG_27:g.46143_46144del

Transcript Alleles

HGVS Amino-acid change
ENST00000695651.1:n.2805-13_2805-12del
ENST00000695653.1:c.2366-13_2366-12del ENSP00000512084.1:n.2366-13_2366-12del
ENST00000695654.1:c.3482-13_3482-12del ENSP00000512085.1:n.3482-13_3482-12del
ENST00000695689.1:c.428-13_428-12del ENSP00000512101.1:n.428-13_428-12del
ENST00000695690.1:n.1522-13_1522-12del
ENST00000695691.1:n.1318-13_1318-12del
ENST00000245907.11:c.4457-13_4457-12del MANE Select ENSP00000245907.4:n.4457-13_4457-12del
ENST00000245907.10:c.4457-13_4457-12del ENSP00000245907.4:n.4457-13_4457-12del
ENST00000599668.1:n.52-13_52-12del
ENST00000599899.5:n.1416-13_1416-12del
ENST00000601008.1:c.242-1551_242-1550del ENSP00000471384.1:n.242-1551_242-1550del
NM_000064.3:c.4457-13_4457-12del NP_000055.2:n.4457-13_4457-12del
NM_000064.4:c.4457-13_4457-12del MANE Select NP_000055.2:n.4457-13_4457-12del
Search 100 bp 5'
Search 100 bp 3'