Canonical Allele Identifier: CA884131895
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs1169258176
gnomAD v3: 19-6713865-A-C
gnomAD v4: 19-6713865-A-C
MyVariant Identifiers: chr19:g.6713876A>C (hg19) chr19:g.6713865A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713865A>C , CM000681.2:g.6713865A>C GRCh38
NC_000019.9:g.6713876A>C , CM000681.1:g.6713876A>C GRCh37
NC_000019.8:g.6664876A>C NCBI36
NG_009557.1:g.11787T>G , LRG_27:g.11787T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.650+127T>G ENSP00000512083.1:n.650+127T>G
ENST00000245907.11:c.773+127T>G MANE Select ENSP00000245907.4:n.773+127T>G
ENST00000245907.10:c.773+127T>G ENSP00000245907.4:n.773+127T>G
ENST00000595577.1:n.277+127T>G
NM_000064.3:c.773+127T>G NP_000055.2:n.773+127T>G
NM_000064.4:c.773+127T>G MANE Select NP_000055.2:n.773+127T>G
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