Canonical Allele Identifier: CA403642814
Gene: C3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.6713517G>C (hg19) chr19:g.6713506G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713506G>C , CM000681.2:g.6713506G>C GRCh38
NC_000019.9:g.6713517G>C , CM000681.1:g.6713517G>C GRCh37
NC_000019.8:g.6664517G>C NCBI36
NG_009557.1:g.12146C>G , LRG_27:g.12146C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.654C>G ENSP00000512083.1:p.Phe218Leu
ENST00000695692.1:n.101C>G
ENST00000245907.11:c.777C>G MANE Select ENSP00000245907.4:p.Phe259Leu
ENST00000245907.10:c.777C>G ENSP00000245907.4:p.Phe259Leu
ENST00000595577.1:n.281C>G
ENST00000597442.5:n.27C>G
NM_000064.3:c.777C>G NP_000055.2:p.Phe259Leu
NM_000064.4:c.777C>G MANE Select NP_000055.2:p.Phe259Leu
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