Canonical Allele Identifier: CA2320550449
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6679501G= , CM000681.2:g.6679501G= GRCh38
NC_000019.9:g.6679512G= , CM000681.1:g.6679512G= GRCh37
NC_000019.8:g.6630512G= NCBI36
NG_009557.1:g.46151C= , LRG_27:g.46151C=

Transcript Alleles

HGVS Amino-acid change
ENST00000695651.1:n.2805-5C=
ENST00000695653.1:c.2366-5C= ENSP00000512084.1:n.2366-5C=
ENST00000695654.1:c.3482-5C= ENSP00000512085.1:n.3482-5C=
ENST00000695689.1:c.428-5C= ENSP00000512101.1:n.428-5C=
ENST00000695690.1:n.1522-5C=
ENST00000695691.1:n.1318-5C=
ENST00000245907.11:c.4457-5C= MANE Select ENSP00000245907.4:n.4457-5C=
ENST00000245907.10:c.4457-5C= ENSP00000245907.4:n.4457-5C=
ENST00000599668.1:n.52-5C=
ENST00000599899.5:n.1416-5C=
ENST00000601008.1:c.242-1543C= ENSP00000471384.1:n.242-1543C=
NM_000064.3:c.4457-5C= NP_000055.2:n.4457-5C=
NM_000064.4:c.4457-5C= MANE Select NP_000055.2:n.4457-5C=