Canonical Allele Identifier: CA2735376326

Gene: C3

Linked Data

• dbSNP Id: rs1568224497

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710025_6710026insAGGGAGAGAGAGGGAGAGAG , CM000681.2:g.6710025_6710026insAGGGAGAGAGAGGGAGAGAG	GRCh38
NC_000019.9:g.6710036_6710037insAGGGAGAGAGAGGGAGAGAG , CM000681.1:g.6710036_6710037insAGGGAGAGAGAGGGAGAGAG	GRCh37
NC_000019.8:g.6661036_6661037insAGGGAGAGAGAGGGAGAGAG	NCBI36
NG_009557.1:g.15627_15628insTCTCTCCCTCTCTCTCCCTC , LRG_27:g.15627_15628insTCTCTCCCTCTCTCTCCCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-183_1564-182insTCTCTCCCTCTCTCTCCCTC	ENSP00000512083.1:n.1564-183_1564-182insTCTCTCCCTCTCTCTCCCTC
ENST00000695654.1:c.811-183_811-182insTCTCTCCCTCTCTCTCCCTC	ENSP00000512085.1:n.811-183_811-182insTCTCTCCCTCTCTCTCCCTC
ENST00000695655.1:c.592-147_592-146insTCTCTCCCTCTCTCTCCCTC	ENSP00000512086.1:n.592-147_592-146insTCTCTCCCTCTCTCTCCCTC
ENST00000695692.1:n.1051-183_1051-182insTCTCTCCCTCTCTCTCCCTC
ENST00000245907.11:c.1687-183_1687-182insTCTCTCCCTCTCTCTCCCTC MANE Select	ENSP00000245907.4:n.1687-183_1687-182insTCTCTCCCTCTCTCTCCCTC
ENST00000245907.10:c.1687-183_1687-182insTCTCTCCCTCTCTCTCCCTC	ENSP00000245907.4:n.1687-183_1687-182insTCTCTCCCTCTCTCTCCCTC
ENST00000600763.1:n.320-183_320-182insTCTCTCCCTCTCTCTCCCTC
NM_000064.3:c.1687-183_1687-182insTCTCTCCCTCTCTCTCCCTC	NP_000055.2:n.1687-183_1687-182insTCTCTCCCTCTCTCTCCCTC
NM_000064.4:c.1687-183_1687-182insTCTCTCCCTCTCTCTCCCTC MANE Select	NP_000055.2:n.1687-183_1687-182insTCTCTCCCTCTCTCTCCCTC