Canonical Allele Identifier: CA2320566049

Gene: C3

Linked Data

• dbSNP Id: rs1967868730
• gnomAD v4: 19-6709968-GGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709976_6709977del , CM000681.2:g.6709976_6709977del	GRCh38
NC_000019.9:g.6709987_6709988del , CM000681.1:g.6709987_6709988del	GRCh37
NC_000019.8:g.6660987_6660988del	NCBI36
NG_009557.1:g.15682_15683del , LRG_27:g.15682_15683del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-128_1564-127del	ENSP00000512083.1:n.1564-128_1564-127del
ENST00000695654.1:c.811-128_811-127del	ENSP00000512085.1:n.811-128_811-127del
ENST00000695655.1:c.592-92_592-91del	ENSP00000512086.1:n.592-92_592-91del
ENST00000695692.1:n.1051-128_1051-127del
ENST00000245907.11:c.1687-128_1687-127del MANE Select	ENSP00000245907.4:n.1687-128_1687-127del
ENST00000245907.10:c.1687-128_1687-127del	ENSP00000245907.4:n.1687-128_1687-127del
ENST00000600763.1:n.320-128_320-127del
NM_000064.3:c.1687-128_1687-127del	NP_000055.2:n.1687-128_1687-127del
NM_000064.4:c.1687-128_1687-127del MANE Select	NP_000055.2:n.1687-128_1687-127del