Canonical Allele Identifier: CA2320572785
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs1968205421

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6722504T>C , CM000681.2:g.6722504T>C GRCh38
NC_000019.9:g.6722515T>C , CM000681.1:g.6722515T>C GRCh37
NC_000019.8:g.6673515T>C NCBI36
NG_009557.1:g.3148A>G , LRG_27:g.3148A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000600744.1:c.-50+937A>G ENSP00000472044.1:n.-50+937A>G