Canonical Allele Identifier: CA403639181

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6709709G>T (hg19) ; chr19:g.6709698G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709698G>T , CM000681.2:g.6709698G>T	GRCh38
NC_000019.9:g.6709709G>T , CM000681.1:g.6709709G>T	GRCh37
NC_000019.8:g.6660709G>T	NCBI36
NG_009557.1:g.15954C>A , LRG_27:g.15954C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1708C>A	ENSP00000512083.1:p.Leu570Met
ENST00000695654.1:c.955C>A	ENSP00000512085.1:p.Leu319Met
ENST00000695655.1:c.772C>A	ENSP00000512086.1:n.772C>A
ENST00000695692.1:n.1195C>A
ENST00000245907.11:c.1831C>A MANE Select	ENSP00000245907.4:p.Leu611Met
ENST00000245907.10:c.1831C>A	ENSP00000245907.4:p.Leu611Met
NM_000064.3:c.1831C>A	NP_000055.2:p.Leu611Met
NM_000064.4:c.1831C>A MANE Select	NP_000055.2:p.Leu611Met