Canonical Allele Identifier: CA993075837

Gene: C3

Linked Data

• dbSNP Id: rs1967951250
• gnomAD v3: 19-6712986-TA-T
• gnomAD v4: 19-6712986-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6712987del , CM000681.2:g.6712987del	GRCh38
NC_000019.9:g.6712998del , CM000681.1:g.6712998del	GRCh37
NC_000019.8:g.6663998del	NCBI36
NG_009557.1:g.12665del , LRG_27:g.12665del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.880+202del	ENSP00000512083.1:n.880+202del
ENST00000695654.1:c.127+202del	ENSP00000512085.1:n.127+202del
ENST00000695692.1:n.327+202del
ENST00000245907.11:c.1003+202del MANE Select	ENSP00000245907.4:n.1003+202del
ENST00000245907.10:c.1003+202del	ENSP00000245907.4:n.1003+202del
ENST00000594270.5:n.127+202del
ENST00000595577.1:n.507+202del
ENST00000597442.5:n.253+202del
NM_000064.3:c.1003+202del	NP_000055.2:n.1003+202del
NM_000064.4:c.1003+202del MANE Select	NP_000055.2:n.1003+202del