Canonical Allele Identifier: CA993073736

Gene: C3

Linked Data

• dbSNP Id: rs1967872368
• gnomAD v3: 19-6710045-G-GAA
• gnomAD v4: 19-6710045-G-GAA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710046_6710047insAA , CM000681.2:g.6710046_6710047insAA	GRCh38
NC_000019.9:g.6710057_6710058insAA , CM000681.1:g.6710057_6710058insAA	GRCh37
NC_000019.8:g.6661057_6661058insAA	NCBI36
NG_009557.1:g.15606_15607insTT , LRG_27:g.15606_15607insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-204_1564-203insTT	ENSP00000512083.1:n.1564-204_1564-203insTT
ENST00000695654.1:c.811-204_811-203insTT	ENSP00000512085.1:n.811-204_811-203insTT
ENST00000695655.1:c.592-168_592-167insTT	ENSP00000512086.1:n.592-168_592-167insTT
ENST00000695692.1:n.1051-204_1051-203insTT
ENST00000245907.11:c.1687-204_1687-203insTT MANE Select	ENSP00000245907.4:n.1687-204_1687-203insTT
ENST00000245907.10:c.1687-204_1687-203insTT	ENSP00000245907.4:n.1687-204_1687-203insTT
ENST00000600763.1:n.320-204_320-203insTT
NM_000064.3:c.1687-204_1687-203insTT	NP_000055.2:n.1687-204_1687-203insTT
NM_000064.4:c.1687-204_1687-203insTT MANE Select	NP_000055.2:n.1687-204_1687-203insTT