Canonical Allele Identifier: CA2587877881
Gene: C3 HGNC NCBI

Linked Data

gnomAD v4: 19-6710849-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6710849G>C , CM000681.2:g.6710849G>C GRCh38
NC_000019.9:g.6710860G>C , CM000681.1:g.6710860G>C GRCh37
NC_000019.8:g.6661860G>C NCBI36
NG_009557.1:g.14803C>G , LRG_27:g.14803C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000695652.1:c.1357-4C>G ENSP00000512083.1:n.1357-4C>G
ENST00000695654.1:c.604-4C>G ENSP00000512085.1:n.604-4C>G
ENST00000695655.1:c.381C>G ENSP00000512086.1:p.Pro127=
ENST00000695692.1:n.844-4C>G
ENST00000245907.11:c.1480-4C>G MANE Select ENSP00000245907.4:n.1480-4C>G
ENST00000245907.10:c.1480-4C>G ENSP00000245907.4:n.1480-4C>G
ENST00000600763.1:n.109C>G
NM_000064.3:c.1480-4C>G NP_000055.2:n.1480-4C>G
NM_000064.4:c.1480-4C>G MANE Select NP_000055.2:n.1480-4C>G