Canonical Allele Identifier: CA403642560
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs1421897305
MyVariant Identifiers: chr19:g.6713453T>C (hg19) chr19:g.6713442T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713442T>C , CM000681.2:g.6713442T>C GRCh38
NC_000019.9:g.6713453T>C , CM000681.1:g.6713453T>C GRCh37
NC_000019.8:g.6664453T>C NCBI36
NG_009557.1:g.12210A>G , LRG_27:g.12210A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.718A>G ENSP00000512083.1:p.Arg240Gly
ENST00000695692.1:n.165A>G
ENST00000245907.11:c.841A>G MANE Select ENSP00000245907.4:p.Arg281Gly
ENST00000245907.10:c.841A>G ENSP00000245907.4:p.Arg281Gly
ENST00000595577.1:n.345A>G
ENST00000597442.5:n.91A>G
NM_000064.3:c.841A>G NP_000055.2:p.Arg281Gly
NM_000064.4:c.841A>G MANE Select NP_000055.2:p.Arg281Gly
Search 100 bp 5'
Search 100 bp 3'