Canonical Allele Identifier: CA403639262

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6709733A>G (hg19) ; chr19:g.6709722A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709722A>G , CM000681.2:g.6709722A>G	GRCh38
NC_000019.9:g.6709733A>G , CM000681.1:g.6709733A>G	GRCh37
NC_000019.8:g.6660733A>G	NCBI36
NG_009557.1:g.15930T>C , LRG_27:g.15930T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1684T>C	ENSP00000512083.1:p.Phe562Leu
ENST00000695654.1:c.931T>C	ENSP00000512085.1:p.Phe311Leu
ENST00000695655.1:c.748T>C	ENSP00000512086.1:n.748T>C
ENST00000695692.1:n.1171T>C
ENST00000245907.11:c.1807T>C MANE Select	ENSP00000245907.4:p.Phe603Leu
ENST00000245907.10:c.1807T>C	ENSP00000245907.4:p.Phe603Leu
NM_000064.3:c.1807T>C	NP_000055.2:p.Phe603Leu
NM_000064.4:c.1807T>C MANE Select	NP_000055.2:p.Phe603Leu