Canonical Allele Identifier: CA403632665

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697392A>C (hg19) ; chr19:g.6697381A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697381A>C , CM000681.2:g.6697381A>C	GRCh38
NC_000019.9:g.6697392A>C , CM000681.1:g.6697392A>C	GRCh37
NC_000019.8:g.6648392A>C	NCBI36
NG_009557.1:g.28271T>G , LRG_27:g.28271T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1107T>G
ENST00000695652.1:c.2636T>G	ENSP00000512083.1:p.Phe879Cys
ENST00000695653.1:c.668T>G	ENSP00000512084.1:p.Phe223Cys
ENST00000695654.1:c.1883T>G	ENSP00000512085.1:p.Phe628Cys
ENST00000695655.1:c.1700T>G	ENSP00000512086.1:n.1700T>G
ENST00000695692.1:n.2123T>G
ENST00000245907.11:c.2759T>G MANE Select	ENSP00000245907.4:p.Phe920Cys
ENST00000245907.10:c.2759T>G	ENSP00000245907.4:p.Phe920Cys
ENST00000594005.1:n.335T>G
NM_000064.3:c.2759T>G	NP_000055.2:p.Phe920Cys
NM_000064.4:c.2759T>G MANE Select	NP_000055.2:p.Phe920Cys