Canonical Allele Identifier: CA403642675
Gene: C3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.6713482A>C (hg19) chr19:g.6713471A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713471A>C , CM000681.2:g.6713471A>C GRCh38
NC_000019.9:g.6713482A>C , CM000681.1:g.6713482A>C GRCh37
NC_000019.8:g.6664482A>C NCBI36
NG_009557.1:g.12181T>G , LRG_27:g.12181T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.689T>G ENSP00000512083.1:p.Val230Gly
ENST00000695692.1:n.136T>G
ENST00000245907.11:c.812T>G MANE Select ENSP00000245907.4:p.Val271Gly
ENST00000245907.10:c.812T>G ENSP00000245907.4:p.Val271Gly
ENST00000595577.1:n.316T>G
ENST00000597442.5:n.62T>G
NM_000064.3:c.812T>G NP_000055.2:p.Val271Gly
NM_000064.4:c.812T>G MANE Select NP_000055.2:p.Val271Gly
Search 100 bp 5'
Search 100 bp 3'