Canonical Allele Identifier: CA403643165
Gene: C3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.6714207A>G (hg19) chr19:g.6714196A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714196A>G , CM000681.2:g.6714196A>G GRCh38
NC_000019.9:g.6714207A>G , CM000681.1:g.6714207A>G GRCh37
NC_000019.8:g.6665207A>G NCBI36
NG_009557.1:g.11456T>C , LRG_27:g.11456T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.529T>C ENSP00000512083.1:p.Phe177Leu
ENST00000245907.11:c.652T>C MANE Select ENSP00000245907.4:p.Phe218Leu
ENST00000245907.10:c.652T>C ENSP00000245907.4:p.Phe218Leu
ENST00000595577.1:n.156T>C
NM_000064.3:c.652T>C NP_000055.2:p.Phe218Leu
NM_000064.4:c.652T>C MANE Select NP_000055.2:p.Phe218Leu
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