Canonical Allele Identifier: CA2320572839
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6722588A= , CM000681.2:g.6722588A= GRCh38
NC_000019.9:g.6722599A= , CM000681.1:g.6722599A= GRCh37
NC_000019.8:g.6673599A= NCBI36
NG_009557.1:g.3064T= , LRG_27:g.3064T=

Transcript Alleles

HGVS Amino-acid change
ENST00000600744.1:c.-50+853T= ENSP00000472044.1:n.-50+853T=