Canonical Allele Identifier: CA403642824
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs1599524950
MyVariant Identifiers: chr19:g.6713519A>C (hg19) chr19:g.6713508A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713508A>C , CM000681.2:g.6713508A>C GRCh38
NC_000019.9:g.6713519A>C , CM000681.1:g.6713519A>C GRCh37
NC_000019.8:g.6664519A>C NCBI36
NG_009557.1:g.12144T>G , LRG_27:g.12144T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.652T>G ENSP00000512083.1:p.Phe218Val
ENST00000695692.1:n.99T>G
ENST00000245907.11:c.775T>G MANE Select ENSP00000245907.4:p.Phe259Val
ENST00000245907.10:c.775T>G ENSP00000245907.4:p.Phe259Val
ENST00000595577.1:n.279T>G
ENST00000597442.5:n.25T>G
NM_000064.3:c.775T>G NP_000055.2:p.Phe259Val
NM_000064.4:c.775T>G MANE Select NP_000055.2:p.Phe259Val
Search 100 bp 5'
Search 100 bp 3'