Canonical Allele Identifier: CA2320551504
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6681898G= , CM000681.2:g.6681898G= GRCh38
NC_000019.9:g.6681909G= , CM000681.1:g.6681909G= GRCh37
NC_000019.8:g.6632909G= NCBI36
NG_009557.1:g.43754C= , LRG_27:g.43754C=

Transcript Alleles

HGVS Amino-acid change
ENST00000695651.1:n.2698+43C=
ENST00000695653.1:c.2259+43C= ENSP00000512084.1:n.2259+43C=
ENST00000695654.1:c.3375+43C= ENSP00000512085.1:n.3375+43C=
ENST00000695689.1:c.321+43C= ENSP00000512101.1:n.321+43C=
ENST00000695690.1:n.584C=
ENST00000695691.1:n.584C=
ENST00000245907.11:c.4350+43C= MANE Select ENSP00000245907.4:n.4350+43C=
ENST00000245907.10:c.4350+43C= ENSP00000245907.4:n.4350+43C=
ENST00000596548.1:c.471+43C= ENSP00000469744.1:n.471+43C=
ENST00000599899.5:n.1309+43C=
ENST00000601008.1:c.242-3940C= ENSP00000471384.1:n.242-3940C=
NM_000064.3:c.4350+43C= NP_000055.2:n.4350+43C=
NM_000064.4:c.4350+43C= MANE Select NP_000055.2:n.4350+43C=