Canonical Allele Identifier: CA2735582594

Gene: C3

Linked Data

• dbSNP Id: rs2145431371

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713671_6713672insGGC , CM000681.2:g.6713671_6713672insGGC	GRCh38
NC_000019.9:g.6713682_6713683insGGC , CM000681.1:g.6713682_6713683insGGC	GRCh37
NC_000019.8:g.6664682_6664683insGGC	NCBI36
NG_009557.1:g.11980_11981insGCC , LRG_27:g.11980_11981insGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.651-163_651-162insGCC	ENSP00000512083.1:n.651-163_651-162insGCC
ENST00000245907.11:c.774-163_774-162insGCC MANE Select	ENSP00000245907.4:n.774-163_774-162insGCC
ENST00000245907.10:c.774-163_774-162insGCC	ENSP00000245907.4:n.774-163_774-162insGCC
ENST00000595577.1:n.278-163_278-162insGCC
ENST00000597442.5:n.23+94_23+95insGCC
NM_000064.3:c.774-163_774-162insGCC	NP_000055.2:n.774-163_774-162insGCC
NM_000064.4:c.774-163_774-162insGCC MANE Select	NP_000055.2:n.774-163_774-162insGCC