Canonical Allele Identifier: CA14633508
Gene: C3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs344550

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6682942C>G , CM000681.2:g.6682942C>G GRCh38
NC_000019.9:g.6682953C>G , CM000681.1:g.6682953C>G GRCh37
NC_000019.8:g.6633953C>G NCBI36
NG_009557.1:g.42710G>C , LRG_27:g.42710G>C

Transcript Alleles

HGVS Amino-acid change
NM_000064.3:c.4173-713G>C VV NP_000055.2:p.=
ENST00000245907.10:c.4173-713G>C ENSP00000245907.4:p.=
ENST00000596548.1:n.294-713G>C ENSP00000469744.1:p.=
ENST00000599899.5:n.419G>C
ENST00000601008.1:n.241+3804G>C ENSP00000471384.1:p.=