Canonical Allele Identifier: CA884131635
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs1478199162
gnomAD v4: 19-6713649-C-T
MyVariant Identifiers: chr19:g.6713660C>T (hg19) chr19:g.6713649C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713649C>T , CM000681.2:g.6713649C>T GRCh38
NC_000019.9:g.6713660C>T , CM000681.1:g.6713660C>T GRCh37
NC_000019.8:g.6664660C>T NCBI36
NG_009557.1:g.12003G>A , LRG_27:g.12003G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.651-140G>A ENSP00000512083.1:n.651-140G>A
ENST00000245907.11:c.774-140G>A MANE Select ENSP00000245907.4:n.774-140G>A
ENST00000245907.10:c.774-140G>A ENSP00000245907.4:n.774-140G>A
ENST00000595577.1:n.278-140G>A
ENST00000597442.5:n.23+117G>A
NM_000064.3:c.774-140G>A NP_000055.2:n.774-140G>A
NM_000064.4:c.774-140G>A MANE Select NP_000055.2:n.774-140G>A
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