Canonical Allele Identifier: CA505124779

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6709758T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709747T>G , CM000681.2:g.6709747T>G	GRCh38
NC_000019.9:g.6709758T>G , CM000681.1:g.6709758T>G	GRCh37
NC_000019.8:g.6660758T>G	NCBI36
NG_009557.1:g.15905A>C , LRG_27:g.15905A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1659A>C	ENSP00000512083.1:p.Val553=
ENST00000695654.1:c.906A>C	ENSP00000512085.1:p.Val302=
ENST00000695655.1:c.723A>C	ENSP00000512086.1:n.723A>C
ENST00000695692.1:n.1146A>C
ENST00000245907.11:c.1782A>C MANE Select	ENSP00000245907.4:p.Val594=
ENST00000245907.10:c.1782A>C	ENSP00000245907.4:p.Val594=
NM_000064.3:c.1782A>C	NP_000055.2:p.Val594=
NM_000064.4:c.1782A>C MANE Select	NP_000055.2:p.Val594=