Canonical Allele Identifier: CA403642688

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6713484A>T (hg19) ; chr19:g.6713473A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713473A>T , CM000681.2:g.6713473A>T	GRCh38
NC_000019.9:g.6713484A>T , CM000681.1:g.6713484A>T	GRCh37
NC_000019.8:g.6664484A>T	NCBI36
NG_009557.1:g.12179T>A , LRG_27:g.12179T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.687T>A	ENSP00000512083.1:p.Phe229Leu
ENST00000695692.1:n.134T>A
ENST00000245907.11:c.810T>A MANE Select	ENSP00000245907.4:p.Phe270Leu
ENST00000245907.10:c.810T>A	ENSP00000245907.4:p.Phe270Leu
ENST00000595577.1:n.314T>A
ENST00000597442.5:n.60T>A
NM_000064.3:c.810T>A	NP_000055.2:p.Phe270Leu
NM_000064.4:c.810T>A MANE Select	NP_000055.2:p.Phe270Leu