Canonical Allele Identifier: CA2320572827
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs1968207330

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6722581_6722583del , CM000681.2:g.6722581_6722583del GRCh38
NC_000019.9:g.6722592_6722594del , CM000681.1:g.6722592_6722594del GRCh37
NC_000019.8:g.6673592_6673594del NCBI36
NG_009557.1:g.3071_3073del , LRG_27:g.3071_3073del

Transcript Alleles

HGVS Amino-acid change
ENST00000600744.1:c.-50+860_-50+862del ENSP00000472044.1:n.-50+860_-50+862del