Canonical Allele Identifier: CA505123398

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6685005T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6684994T>C , CM000681.2:g.6684994T>C	GRCh38
NC_000019.9:g.6685005T>C , CM000681.1:g.6685005T>C	GRCh37
NC_000019.8:g.6636005T>C	NCBI36
NG_009557.1:g.40658A>G , LRG_27:g.40658A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2311A>G
ENST00000695653.1:c.1872A>G	ENSP00000512084.1:p.Ser624=
ENST00000695654.1:c.2988A>G	ENSP00000512085.1:p.Ser996=
ENST00000695690.1:n.154A>G
ENST00000695691.1:n.154A>G
ENST00000245907.11:c.3963A>G MANE Select	ENSP00000245907.4:p.Ser1321=
ENST00000245907.10:c.3963A>G	ENSP00000245907.4:p.Ser1321=
ENST00000596238.1:n.406A>G
ENST00000596548.1:c.45A>G	ENSP00000469744.1:p.Ser15=
ENST00000601008.1:c.241+1752A>G	ENSP00000471384.1:n.241+1752A>G
NM_000064.3:c.3963A>G	NP_000055.2:p.Ser1321=
NM_000064.4:c.3963A>G MANE Select	NP_000055.2:p.Ser1321=