Canonical Allele Identifier: CA403642524
Gene: C3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.6713444G>C (hg19) chr19:g.6713433G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713433G>C , CM000681.2:g.6713433G>C GRCh38
NC_000019.9:g.6713444G>C , CM000681.1:g.6713444G>C GRCh37
NC_000019.8:g.6664444G>C NCBI36
NG_009557.1:g.12219C>G , LRG_27:g.12219C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.727C>G ENSP00000512083.1:p.Leu243Val
ENST00000695692.1:n.174C>G
ENST00000245907.11:c.850C>G MANE Select ENSP00000245907.4:p.Leu284Val
ENST00000245907.10:c.850C>G ENSP00000245907.4:p.Leu284Val
ENST00000595577.1:n.354C>G
ENST00000597442.5:n.100C>G
NM_000064.3:c.850C>G NP_000055.2:p.Leu284Val
NM_000064.4:c.850C>G MANE Select NP_000055.2:p.Leu284Val
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