Canonical Allele Identifier: CA2320567893
Gene: C3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713375G= , CM000681.2:g.6713375G= GRCh38
NC_000019.9:g.6713386G= , CM000681.1:g.6713386G= GRCh37
NC_000019.8:g.6664386G= NCBI36
NG_009557.1:g.12277C= , LRG_27:g.12277C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.753+32C= ENSP00000512083.1:n.753+32C=
ENST00000695692.1:n.200+32C=
ENST00000245907.11:c.876+32C= MANE Select ENSP00000245907.4:n.876+32C=
ENST00000245907.10:c.876+32C= ENSP00000245907.4:n.876+32C=
ENST00000595577.1:n.380+32C=
ENST00000597442.5:n.126+32C=
NM_000064.3:c.876+32C= NP_000055.2:n.876+32C=
NM_000064.4:c.876+32C= MANE Select NP_000055.2:n.876+32C=
Search 100 bp 5'
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