Canonical Allele Identifier: CA2320559248
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6697834G= , CM000681.2:g.6697834G= GRCh38
NC_000019.9:g.6697845G= , CM000681.1:g.6697845G= GRCh37
NC_000019.8:g.6648845G= NCBI36
NG_009557.1:g.27818C= , LRG_27:g.27818C=

Transcript Alleles

HGVS Amino-acid change
ENST00000695651.1:n.789-40C=
ENST00000695652.1:c.2318-40C= ENSP00000512083.1:n.2318-40C=
ENST00000695653.1:c.350-40C= ENSP00000512084.1:n.350-40C=
ENST00000695654.1:c.1565-40C= ENSP00000512085.1:n.1565-40C=
ENST00000695655.1:c.1382-40C= ENSP00000512086.1:n.1382-40C=
ENST00000695692.1:n.1805-40C=
ENST00000245907.11:c.2441-40C= MANE Select ENSP00000245907.4:n.2441-40C=
ENST00000245907.10:c.2441-40C= ENSP00000245907.4:n.2441-40C=
ENST00000602053.1:n.489-40C=
NM_000064.3:c.2441-40C= NP_000055.2:n.2441-40C=
NM_000064.4:c.2441-40C= MANE Select NP_000055.2:n.2441-40C=