Canonical Allele Identifier: CA505192557

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697750G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697739G>A , CM000681.2:g.6697739G>A	GRCh38
NC_000019.9:g.6697750G>A , CM000681.1:g.6697750G>A	GRCh37
NC_000019.8:g.6648750G>A	NCBI36
NG_009557.1:g.27913C>T , LRG_27:g.27913C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.844C>T
ENST00000695652.1:c.2373C>T	ENSP00000512083.1:p.Asp791=
ENST00000695653.1:c.405C>T	ENSP00000512084.1:p.Asp135=
ENST00000695654.1:c.1620C>T	ENSP00000512085.1:p.Asp540=
ENST00000695655.1:c.1437C>T	ENSP00000512086.1:n.1437C>T
ENST00000695692.1:n.1860C>T
ENST00000245907.11:c.2496C>T MANE Select	ENSP00000245907.4:p.Asp832=
ENST00000245907.10:c.2496C>T	ENSP00000245907.4:p.Asp832=
ENST00000602053.1:n.544C>T
NM_000064.3:c.2496C>T	NP_000055.2:p.Asp832=
NM_000064.4:c.2496C>T MANE Select	NP_000055.2:p.Asp832=