Canonical Allele Identifier: CA403643696
Gene: C3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.6714455G>T (hg19) chr19:g.6714444G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714444G>T , CM000681.2:g.6714444G>T GRCh38
NC_000019.9:g.6714455G>T , CM000681.1:g.6714455G>T GRCh37
NC_000019.8:g.6665455G>T NCBI36
NG_009557.1:g.11208C>A , LRG_27:g.11208C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.384C>A ENSP00000512083.1:p.Asn128Lys
ENST00000245907.11:c.507C>A MANE Select ENSP00000245907.4:p.Asn169Lys
ENST00000245907.10:c.507C>A ENSP00000245907.4:p.Asn169Lys
NM_000064.3:c.507C>A NP_000055.2:p.Asn169Lys
NM_000064.4:c.507C>A MANE Select NP_000055.2:p.Asn169Lys
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