Canonical Allele Identifier: CA2320559236
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6697818G= , CM000681.2:g.6697818G= GRCh38
NC_000019.9:g.6697829G= , CM000681.1:g.6697829G= GRCh37
NC_000019.8:g.6648829G= NCBI36
NG_009557.1:g.27834C= , LRG_27:g.27834C=

Transcript Alleles

HGVS Amino-acid change
ENST00000695651.1:n.789-24C=
ENST00000695652.1:c.2318-24C= ENSP00000512083.1:n.2318-24C=
ENST00000695653.1:c.350-24C= ENSP00000512084.1:n.350-24C=
ENST00000695654.1:c.1565-24C= ENSP00000512085.1:n.1565-24C=
ENST00000695655.1:c.1382-24C= ENSP00000512086.1:n.1382-24C=
ENST00000695692.1:n.1805-24C=
ENST00000245907.11:c.2441-24C= MANE Select ENSP00000245907.4:n.2441-24C=
ENST00000245907.10:c.2441-24C= ENSP00000245907.4:n.2441-24C=
ENST00000602053.1:n.489-24C=
NM_000064.3:c.2441-24C= NP_000055.2:n.2441-24C=
NM_000064.4:c.2441-24C= MANE Select NP_000055.2:n.2441-24C=