Canonical Allele Identifier: CA993073563

Gene: C3

Linked Data

• gnomAD v3: 19-6710016-GGAGAGAGGGCGGGA-G
• gnomAD v4: 19-6710016-GGAGAGAGGGCGGGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710024_6710037del , CM000681.2:g.6710024_6710037del	GRCh38
NC_000019.9:g.6710035_6710048del , CM000681.1:g.6710035_6710048del	GRCh37
NC_000019.8:g.6661035_6661048del	NCBI36
NG_009557.1:g.15622_15635del , LRG_27:g.15622_15635del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-188_1564-175del	ENSP00000512083.1:n.1564-188_1564-175del
ENST00000695654.1:c.811-188_811-175del	ENSP00000512085.1:n.811-188_811-175del
ENST00000695655.1:c.592-152_592-139del	ENSP00000512086.1:n.592-152_592-139del
ENST00000695692.1:n.1051-188_1051-175del
ENST00000245907.11:c.1687-188_1687-175del MANE Select	ENSP00000245907.4:n.1687-188_1687-175del
ENST00000245907.10:c.1687-188_1687-175del	ENSP00000245907.4:n.1687-188_1687-175del
ENST00000600763.1:n.320-188_320-175del
NM_000064.3:c.1687-188_1687-175del	NP_000055.2:n.1687-188_1687-175del
NM_000064.4:c.1687-188_1687-175del MANE Select	NP_000055.2:n.1687-188_1687-175del