Canonical Allele Identifier: CA2735582593
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs2145431355

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713668_6713669insTCACCTGGCGGTGATGGTGACCT , CM000681.2:g.6713668_6713669insTCACCTGGCGGTGATGGTGACCT GRCh38
NC_000019.9:g.6713679_6713680insTCACCTGGCGGTGATGGTGACCT , CM000681.1:g.6713679_6713680insTCACCTGGCGGTGATGGTGACCT GRCh37
NC_000019.8:g.6664679_6664680insTCACCTGGCGGTGATGGTGACCT NCBI36
NG_009557.1:g.11983_11984insAGGTCACCATCACCGCCAGGTGA , LRG_27:g.11983_11984insAGGTCACCATCACCGCCAGGTGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.651-160_651-159insAGGTCACCATCACCGCCAGGTGA ENSP00000512083.1:n.651-160_651-159insAGGTCACCATCACCGCCAGGTGA...
ENST00000245907.11:c.774-160_774-159insAGGTCACCATCACCGCCAGGTGA MANE Select ENSP00000245907.4:n.774-160_774-159insAGGTCACCATCACCGCCAGGTGA...
ENST00000245907.10:c.774-160_774-159insAGGTCACCATCACCGCCAGGTGA ENSP00000245907.4:n.774-160_774-159insAGGTCACCATCACCGCCAGGTGA...
ENST00000595577.1:n.278-160_278-159insAGGTCACCATCACCGCCAGGTGA
ENST00000597442.5:n.23+97_23+98insAGGTCACCATCACCGCCAGGTGA
NM_000064.3:c.774-160_774-159insAGGTCACCATCACCGCCAGGTGA NP_000055.2:n.774-160_774-159insAGGTCACCATCACCGCCAGGTGA
NM_000064.4:c.774-160_774-159insAGGTCACCATCACCGCCAGGTGA MANE Select NP_000055.2:n.774-160_774-159insAGGTCACCATCACCGCCAGGTGA