Canonical Allele Identifier: CA2320572840
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs1568231570

Genomic Alleles

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

Transcript Alleles

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