Canonical Allele Identifier: CA2320553339
Gene: C3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6685942G= , CM000681.2:g.6685942G= GRCh38
NC_000019.9:g.6685953G= , CM000681.1:g.6685953G= GRCh37
NC_000019.8:g.6636953G= NCBI36
NG_009557.1:g.39710C= , LRG_27:g.39710C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695651.1:n.2158+182C=
ENST00000695653.1:c.1719+182C= ENSP00000512084.1:n.1719+182C=
ENST00000695654.1:c.2835+182C= ENSP00000512085.1:n.2835+182C=
ENST00000245907.11:c.3810+182C= MANE Select ENSP00000245907.4:n.3810+182C=
ENST00000245907.10:c.3810+182C= ENSP00000245907.4:n.3810+182C=
ENST00000596238.1:n.253+182C=
ENST00000601008.1:c.241+804C= ENSP00000471384.1:n.241+804C=
NM_000064.3:c.3810+182C= NP_000055.2:n.3810+182C=
NM_000064.4:c.3810+182C= MANE Select NP_000055.2:n.3810+182C=
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