Canonical Allele Identifier: CA403632667

Gene: C3

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1107T>C
ENST00000695652.1:c.2636T>C	ENSP00000512083.1:p.Phe879Ser
ENST00000695653.1:c.668T>C	ENSP00000512084.1:p.Phe223Ser
ENST00000695654.1:c.1883T>C	ENSP00000512085.1:p.Phe628Ser
ENST00000695655.1:c.1700T>C	ENSP00000512086.1:n.1700T>C
ENST00000695692.1:n.2123T>C
ENST00000245907.11:c.2759T>C MANE Select	ENSP00000245907.4:p.Phe920Ser
ENST00000245907.10:c.2759T>C	ENSP00000245907.4:p.Phe920Ser
ENST00000594005.1:n.335T>C
NM_000064.3:c.2759T>C	NP_000055.2:p.Phe920Ser
NM_000064.4:c.2759T>C MANE Select	NP_000055.2:p.Phe920Ser