Canonical Allele Identifier: CA14633511
Gene: C3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2241392

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6685972G>C , CM000681.2:g.6685972G>C GRCh38
NC_000019.9:g.6685983G>C , CM000681.1:g.6685983G>C GRCh37
NC_000019.8:g.6636983G>C NCBI36
NG_009557.1:g.39680C>G , LRG_27:g.39680C>G

Transcript Alleles

HGVS Amino-acid change
NM_000064.3:c.3810+152C>G VV NP_000055.2:p.=
ENST00000245907.10:c.3810+152C>G ENSP00000245907.4:p.=
ENST00000596238.1:n.253+152C>G
ENST00000601008.1:n.241+774C>G ENSP00000471384.1:p.=