Canonical Allele Identifier: CA645620273
Gene: C3 HGNC NCBI

Linked Data

COSMIC: COSM6293307
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713398C>A , CM000681.2:g.6713398C>A GRCh38
NC_000019.9:g.6713409C>A , CM000681.1:g.6713409C>A GRCh37
NC_000019.8:g.6664409C>A NCBI36
NG_009557.1:g.12254G>T , LRG_27:g.12254G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.753+9G>T ENSP00000512083.1:n.753+9G>T
ENST00000695692.1:n.200+9G>T
ENST00000245907.11:c.876+9G>T MANE Select ENSP00000245907.4:n.876+9G>T
ENST00000245907.10:c.876+9G>T ENSP00000245907.4:n.876+9G>T
ENST00000595577.1:n.380+9G>T
ENST00000597442.5:n.126+9G>T
NM_000064.3:c.876+9G>T NP_000055.2:n.876+9G>T
NM_000064.4:c.876+9G>T MANE Select NP_000055.2:n.876+9G>T
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