Canonical Allele Identifier: CA2320572861
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6722611_6722613delinsATC , CM000681.2:g.6722611_6722613delinsATC GRCh38
NC_000019.9:g.6722622_6722624delinsATC , CM000681.1:g.6722622_6722624delinsATC GRCh37
NC_000019.8:g.6673622_6673624delinsATC NCBI36
NG_009557.1:g.3039_3041delinsGAT , LRG_27:g.3039_3041delinsGAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000600744.1:c.-50+828_-50+830delinsGAT ENSP00000472044.1:n.-50+828_-50+830delinsGAT