Canonical Allele Identifier: CA403639599

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6709835G>T (hg19) ; chr19:g.6709824G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709824G>T , CM000681.2:g.6709824G>T	GRCh38
NC_000019.9:g.6709835G>T , CM000681.1:g.6709835G>T	GRCh37
NC_000019.8:g.6660835G>T	NCBI36
NG_009557.1:g.15828C>A , LRG_27:g.15828C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1582C>A	ENSP00000512083.1:p.Gln528Lys
ENST00000695654.1:c.829C>A	ENSP00000512085.1:p.Gln277Lys
ENST00000695655.1:c.646C>A	ENSP00000512086.1:n.646C>A
ENST00000695692.1:n.1069C>A
ENST00000245907.11:c.1705C>A MANE Select	ENSP00000245907.4:p.Gln569Lys
ENST00000245907.10:c.1705C>A	ENSP00000245907.4:p.Gln569Lys
ENST00000600763.1:n.338C>A
NM_000064.3:c.1705C>A	NP_000055.2:p.Gln569Lys
NM_000064.4:c.1705C>A MANE Select	NP_000055.2:p.Gln569Lys