Canonical Allele Identifier: CA9129661
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs764388528
ExAC: 19:6713488 G / A
gnomAD v2: 19-6713488-G-A
MyVariant Identifiers: chr19:g.6713488G>A (hg19) chr19:g.6713477G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713477G>A , CM000681.2:g.6713477G>A GRCh38
NC_000019.9:g.6713488G>A , CM000681.1:g.6713488G>A GRCh37
NC_000019.8:g.6664488G>A NCBI36
NG_009557.1:g.12175C>T , LRG_27:g.12175C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.683C>T ENSP00000512083.1:p.Ala228Val
ENST00000695692.1:n.130C>T
ENST00000245907.11:c.806C>T MANE Select ENSP00000245907.4:p.Ala269Val
ENST00000245907.10:c.806C>T ENSP00000245907.4:p.Ala269Val
ENST00000595577.1:n.310C>T
ENST00000597442.5:n.56C>T
NM_000064.3:c.806C>T NP_000055.2:p.Ala269Val
NM_000064.4:c.806C>T MANE Select NP_000055.2:p.Ala269Val
Search 100 bp 5'
Search 100 bp 3'