Canonical Allele Identifier: CA403645253

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6718366G>T (hg19) ; chr19:g.6718355G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6718355G>T , CM000681.2:g.6718355G>T	GRCh38
NC_000019.9:g.6718366G>T , CM000681.1:g.6718366G>T	GRCh37
NC_000019.8:g.6669366G>T	NCBI36
NG_009557.1:g.7297C>A , LRG_27:g.7297C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000594936.2:n.386C>A
ENST00000695652.1:c.202C>A	ENSP00000512083.1:p.Gln68Lys
ENST00000695693.1:c.325C>A	ENSP00000512104.1:p.Gln109Lys
ENST00000245907.11:c.325C>A MANE Select	ENSP00000245907.4:p.Gln109Lys
ENST00000245907.10:c.325C>A	ENSP00000245907.4:p.Gln109Lys
ENST00000594936.1:n.386C>A
ENST00000600744.1:c.202C>A	ENSP00000472044.1:p.Gln68Lys
NM_000064.3:c.325C>A	NP_000055.2:p.Gln109Lys
NM_000064.4:c.325C>A MANE Select	NP_000055.2:p.Gln109Lys