Canonical Allele Identifier: CA884131734
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs1437885826
gnomAD v3: 19-6713716-T-C
gnomAD v4: 19-6713716-T-C
MyVariant Identifiers: chr19:g.6713727T>C (hg19) chr19:g.6713716T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713716T>C , CM000681.2:g.6713716T>C GRCh38
NC_000019.9:g.6713727T>C , CM000681.1:g.6713727T>C GRCh37
NC_000019.8:g.6664727T>C NCBI36
NG_009557.1:g.11936A>G , LRG_27:g.11936A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.651-207A>G ENSP00000512083.1:n.651-207A>G
ENST00000245907.11:c.774-207A>G MANE Select ENSP00000245907.4:n.774-207A>G
ENST00000245907.10:c.774-207A>G ENSP00000245907.4:n.774-207A>G
ENST00000595577.1:n.278-207A>G
ENST00000597442.5:n.23+50A>G
NM_000064.3:c.774-207A>G NP_000055.2:n.774-207A>G
NM_000064.4:c.774-207A>G MANE Select NP_000055.2:n.774-207A>G
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