Canonical Allele Identifier: CA9129667
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs544022937
ExAC: 19:6713523 A / G
gnomAD v2: 19-6713523-A-G
gnomAD v3: 19-6713512-A-G
gnomAD v4: 19-6713512-A-G
MyVariant Identifiers: chr19:g.6713523A>G (hg19) chr19:g.6713512A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713512A>G , CM000681.2:g.6713512A>G GRCh38
NC_000019.9:g.6713523A>G , CM000681.1:g.6713523A>G GRCh37
NC_000019.8:g.6664523A>G NCBI36
NG_009557.1:g.12140T>C , LRG_27:g.12140T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.651-3T>C ENSP00000512083.1:n.651-3T>C
ENST00000695692.1:n.95T>C
ENST00000245907.11:c.774-3T>C MANE Select ENSP00000245907.4:n.774-3T>C
ENST00000245907.10:c.774-3T>C ENSP00000245907.4:n.774-3T>C
ENST00000595577.1:n.278-3T>C
ENST00000597442.5:n.24-3T>C
NM_000064.3:c.774-3T>C NP_000055.2:n.774-3T>C
NM_000064.4:c.774-3T>C MANE Select NP_000055.2:n.774-3T>C
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