Canonical Allele Identifier: CA2320568452
Gene: C3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714163T= , CM000681.2:g.6714163T= GRCh38
NC_000019.9:g.6714174T= , CM000681.1:g.6714174T= GRCh37
NC_000019.8:g.6665174T= NCBI36
NG_009557.1:g.11489A= , LRG_27:g.11489A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.559+3A= ENSP00000512083.1:n.559+3A=
ENST00000245907.11:c.682+3A= MANE Select ENSP00000245907.4:n.682+3A=
ENST00000245907.10:c.682+3A= ENSP00000245907.4:n.682+3A=
ENST00000595577.1:n.186+3A=
NM_000064.3:c.682+3A= NP_000055.2:n.682+3A=
NM_000064.4:c.682+3A= MANE Select NP_000055.2:n.682+3A=
Search 100 bp 5'
Search 100 bp 3'