Canonical Allele Identifier: CA993075760
Gene: C3 HGNC NCBI

Linked Data

gnomAD v3: 19-6712774-T-C
gnomAD v4: 19-6712774-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6712774T>C , CM000681.2:g.6712774T>C GRCh38
NC_000019.9:g.6712785T>C , CM000681.1:g.6712785T>C GRCh37
NC_000019.8:g.6663785T>C NCBI36
NG_009557.1:g.12878A>G , LRG_27:g.12878A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.881-151A>G ENSP00000512083.1:n.881-151A>G
ENST00000695654.1:c.128-151A>G ENSP00000512085.1:n.128-151A>G
ENST00000695692.1:n.328-111A>G
ENST00000245907.11:c.1004-151A>G MANE Select ENSP00000245907.4:n.1004-151A>G
ENST00000245907.10:c.1004-151A>G ENSP00000245907.4:n.1004-151A>G
ENST00000594270.5:n.128-172A>G
ENST00000595577.1:n.508-151A>G
ENST00000597442.5:n.254-151A>G
NM_000064.3:c.1004-151A>G NP_000055.2:n.1004-151A>G
NM_000064.4:c.1004-151A>G MANE Select NP_000055.2:n.1004-151A>G
Search 100 bp 5'
Search 100 bp 3'