Canonical Allele Identifier: CA14653451
Gene: C3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs445750

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6701502G>A , CM000681.2:g.6701502G>A GRCh38
NC_000019.9:g.6701513G>A , CM000681.1:g.6701513G>A GRCh37
NC_000019.8:g.6652513G>A NCBI36
NG_009557.1:g.24150C>T , LRG_27:g.24150C>T

Transcript Alleles

HGVS Amino-acid change
NM_000064.3:c.2440+625C>T VV NP_000055.2:p.=
ENST00000245907.10:c.2440+625C>T ENSP00000245907.4:p.=
ENST00000602053.1:n.488+625C>T