Canonical Allele Identifier: CA9129065
Gene: C3 HGNC NCBI
MyVariant.info:
GRCh38 chr19:g.6697818G>T
GRCh37 chr19:g.6697829G>T
gnomAD v2:
19:6697829 G / T
gnomAD v3:
19:6697818 G / T
gnomAD v4:
chr19-6697818-G-T
Joint Max Group AF 0.85501313 (EAS)
Genomes Max Group AF 0.81986389 (EAS)
Exomes Max Group AF 0.85733737 (EAS)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6697818G>T , CM000681.2:g.6697818G>T GRCh38
NC_000019.9:g.6697829G>T , CM000681.1:g.6697829G>T GRCh37
NC_000019.8:g.6648829G>T NCBI36
NG_009557.1:g.27834C>A , LRG_27:g.27834C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695651.1:n.789-24C>A
ENST00000695652.1:c.2318-24C>A ENSP00000512083.1:n.2318-24C>A
ENST00000695653.1:c.350-24C>A ENSP00000512084.1:n.350-24C>A
ENST00000695654.1:c.1565-24C>A ENSP00000512085.1:n.1565-24C>A
ENST00000695655.1:c.1382-24C>A ENSP00000512086.1:n.1382-24C>A
ENST00000695692.1:n.1805-24C>A
ENST00000245907.11:c.2441-24C>A MANE Select ENSP00000245907.4:n.2441-24C>A
ENST00000245907.10:c.2441-24C>A ENSP00000245907.4:n.2441-24C>A
ENST00000602053.1:n.489-24C>A
NM_000064.3:c.2441-24C>A NP_000055.2:n.2441-24C>A
NM_000064.4:c.2441-24C>A MANE Select NP_000055.2:n.2441-24C>A
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