Canonical Allele Identifier: CA304803778
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs923244565
MyVariant Identifiers: chr19:g.6718465C>T (hg19) chr19:g.6718454C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6718454C>T , CM000681.2:g.6718454C>T GRCh38
NC_000019.9:g.6718465C>T , CM000681.1:g.6718465C>T GRCh37
NC_000019.8:g.6669465C>T NCBI36
NG_009557.1:g.7198G>A , LRG_27:g.7198G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000594936.2:n.329-42G>A
ENST00000695652.1:c.145-42G>A ENSP00000512083.1:n.145-42G>A
ENST00000695693.1:c.268-42G>A ENSP00000512104.1:n.268-42G>A
ENST00000245907.11:c.268-42G>A MANE Select ENSP00000245907.4:n.268-42G>A
ENST00000245907.10:c.268-42G>A ENSP00000245907.4:n.268-42G>A
ENST00000594936.1:n.329-42G>A
ENST00000600744.1:c.145-42G>A ENSP00000472044.1:n.145-42G>A
NM_000064.3:c.268-42G>A NP_000055.2:n.268-42G>A
NM_000064.4:c.268-42G>A MANE Select NP_000055.2:n.268-42G>A
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