Canonical Allele Identifier: CA505123722

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6686261G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686250G>A , CM000681.2:g.6686250G>A	GRCh38
NC_000019.9:g.6686261G>A , CM000681.1:g.6686261G>A	GRCh37
NC_000019.8:g.6637261G>A	NCBI36
NG_009557.1:g.39402C>T , LRG_27:g.39402C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2032C>T
ENST00000695652.1:c.3561C>T	ENSP00000512083.1:p.Tyr1187=
ENST00000695653.1:c.1593C>T	ENSP00000512084.1:p.Tyr531=
ENST00000695654.1:c.2709C>T	ENSP00000512085.1:p.Tyr903=
ENST00000695655.1:c.2625C>T	ENSP00000512086.1:n.2625C>T
ENST00000695692.1:n.3048C>T
ENST00000245907.11:c.3684C>T MANE Select	ENSP00000245907.4:p.Tyr1228=
ENST00000245907.10:c.3684C>T	ENSP00000245907.4:p.Tyr1228=
ENST00000596238.1:n.127C>T
ENST00000601008.1:c.241+496C>T	ENSP00000471384.1:n.241+496C>T
NM_000064.3:c.3684C>T	NP_000055.2:p.Tyr1228=
NM_000064.4:c.3684C>T MANE Select	NP_000055.2:p.Tyr1228=