Canonical Allele Identifier: CA2320552785

Gene: C3

Linked Data

• dbSNP Id: rs1917959395

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6684853_6684854del , CM000681.2:g.6684853_6684854del	GRCh38
NC_000019.9:g.6684864_6684865del , CM000681.1:g.6684864_6684865del	GRCh37
NC_000019.8:g.6635864_6635865del	NCBI36
NG_009557.1:g.40803_40804del , LRG_27:g.40803_40804del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2318-15_2318-14del
ENST00000695653.1:c.1879-15_1879-14del	ENSP00000512084.1:n.1879-15_1879-14del
ENST00000695654.1:c.2995-15_2995-14del	ENSP00000512085.1:n.2995-15_2995-14del
ENST00000695690.1:n.161-15_161-14del
ENST00000695691.1:n.161-15_161-14del
ENST00000245907.11:c.3970-15_3970-14del MANE Select	ENSP00000245907.4:n.3970-15_3970-14del
ENST00000245907.10:c.3970-15_3970-14del	ENSP00000245907.4:n.3970-15_3970-14del
ENST00000596238.1:n.413-15_413-14del
ENST00000596548.1:c.52-15_52-14del	ENSP00000469744.1:n.52-15_52-14del
ENST00000601008.1:c.241+1897_241+1898del	ENSP00000471384.1:n.241+1897_241+1898del
NM_000064.3:c.3970-15_3970-14del	NP_000055.2:n.3970-15_3970-14del
NM_000064.4:c.3970-15_3970-14del MANE Select	NP_000055.2:n.3970-15_3970-14del