Canonical Allele Identifier: CA2320572800
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6722535T= , CM000681.2:g.6722535T= GRCh38
NC_000019.9:g.6722546T= , CM000681.1:g.6722546T= GRCh37
NC_000019.8:g.6673546T= NCBI36
NG_009557.1:g.3117A= , LRG_27:g.3117A=

Transcript Alleles

HGVS Amino-acid change
ENST00000600744.1:c.-50+906A= ENSP00000472044.1:n.-50+906A=