Canonical Allele Identifier: CA2320559244
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6697831C= , CM000681.2:g.6697831C= GRCh38
NC_000019.9:g.6697842C= , CM000681.1:g.6697842C= GRCh37
NC_000019.8:g.6648842C= NCBI36
NG_009557.1:g.27821G= , LRG_27:g.27821G=

Transcript Alleles

HGVS Amino-acid change
ENST00000695651.1:n.789-37G=
ENST00000695652.1:c.2318-37G= ENSP00000512083.1:n.2318-37G=
ENST00000695653.1:c.350-37G= ENSP00000512084.1:n.350-37G=
ENST00000695654.1:c.1565-37G= ENSP00000512085.1:n.1565-37G=
ENST00000695655.1:c.1382-37G= ENSP00000512086.1:n.1382-37G=
ENST00000695692.1:n.1805-37G=
ENST00000245907.11:c.2441-37G= MANE Select ENSP00000245907.4:n.2441-37G=
ENST00000245907.10:c.2441-37G= ENSP00000245907.4:n.2441-37G=
ENST00000602053.1:n.489-37G=
NM_000064.3:c.2441-37G= NP_000055.2:n.2441-37G=
NM_000064.4:c.2441-37G= MANE Select NP_000055.2:n.2441-37G=