Canonical Allele Identifier: CA2587878372
Gene: C3 HGNC NCBI

Linked Data

gnomAD v4: 19-6713545-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713545C>T , CM000681.2:g.6713545C>T GRCh38
NC_000019.9:g.6713556C>T , CM000681.1:g.6713556C>T GRCh37
NC_000019.8:g.6664556C>T NCBI36
NG_009557.1:g.12107G>A , LRG_27:g.12107G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.651-36G>A ENSP00000512083.1:n.651-36G>A
ENST00000695692.1:n.62G>A
ENST00000245907.11:c.774-36G>A MANE Select ENSP00000245907.4:n.774-36G>A
ENST00000245907.10:c.774-36G>A ENSP00000245907.4:n.774-36G>A
ENST00000595577.1:n.278-36G>A
ENST00000597442.5:n.24-36G>A
NM_000064.3:c.774-36G>A NP_000055.2:n.774-36G>A
NM_000064.4:c.774-36G>A MANE Select NP_000055.2:n.774-36G>A
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