Canonical Allele Identifier: CA2587873930
Gene: C3 HGNC NCBI

Linked Data

gnomAD v4: 19-6690609-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6690609G>C , CM000681.2:g.6690609G>C GRCh38
NC_000019.9:g.6690620G>C , CM000681.1:g.6690620G>C GRCh37
NC_000019.8:g.6641620G>C NCBI36
NG_009557.1:g.35043C>G , LRG_27:g.35043C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000695651.1:n.1837+20C>G
ENST00000695652.1:c.3366+20C>G ENSP00000512083.1:n.3366+20C>G
ENST00000695653.1:c.1398+20C>G ENSP00000512084.1:n.1398+20C>G
ENST00000695654.1:c.2514+2315C>G ENSP00000512085.1:n.2514+2315C>G
ENST00000695655.1:c.2430+20C>G ENSP00000512086.1:n.2430+20C>G
ENST00000695692.1:n.2853+20C>G
ENST00000245907.11:c.3489+20C>G MANE Select ENSP00000245907.4:n.3489+20C>G
ENST00000245907.10:c.3489+20C>G ENSP00000245907.4:n.3489+20C>G
ENST00000598805.2:n.259+20C>G
ENST00000601008.1:c.84+20C>G ENSP00000471384.1:n.84+20C>G
NM_000064.3:c.3489+20C>G NP_000055.2:n.3489+20C>G
NM_000064.4:c.3489+20C>G MANE Select NP_000055.2:n.3489+20C>G