Canonical Allele Identifier: CA403632853

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697432G>C (hg19) ; chr19:g.6697421G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697421G>C , CM000681.2:g.6697421G>C	GRCh38
NC_000019.9:g.6697432G>C , CM000681.1:g.6697432G>C	GRCh37
NC_000019.8:g.6648432G>C	NCBI36
NG_009557.1:g.28231C>G , LRG_27:g.28231C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1067C>G
ENST00000695652.1:c.2596C>G	ENSP00000512083.1:p.Leu866Val
ENST00000695653.1:c.628C>G	ENSP00000512084.1:p.Leu210Val
ENST00000695654.1:c.1843C>G	ENSP00000512085.1:p.Leu615Val
ENST00000695655.1:c.1660C>G	ENSP00000512086.1:n.1660C>G
ENST00000695692.1:n.2083C>G
ENST00000245907.11:c.2719C>G MANE Select	ENSP00000245907.4:p.Leu907Val
ENST00000245907.10:c.2719C>G	ENSP00000245907.4:p.Leu907Val
ENST00000594005.1:n.295C>G
NM_000064.3:c.2719C>G	NP_000055.2:p.Leu907Val
NM_000064.4:c.2719C>G MANE Select	NP_000055.2:p.Leu907Val