Canonical Allele Identifier: CA505120486

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6679479C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679468C>A , CM000681.2:g.6679468C>A	GRCh38
NC_000019.9:g.6679479C>A , CM000681.1:g.6679479C>A	GRCh37
NC_000019.8:g.6630479C>A	NCBI36
NG_009557.1:g.46184G>T , LRG_27:g.46184G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2833G>T
ENST00000695653.1:c.2394G>T	ENSP00000512084.1:p.Pro798=
ENST00000695654.1:c.3510G>T	ENSP00000512085.1:p.Pro1170=
ENST00000695689.1:c.456G>T	ENSP00000512101.1:n.456G>T
ENST00000695690.1:n.1550G>T
ENST00000695691.1:n.1346G>T
ENST00000245907.11:c.4485G>T MANE Select	ENSP00000245907.4:p.Pro1495=
ENST00000245907.10:c.4485G>T	ENSP00000245907.4:p.Pro1495=
ENST00000599668.1:n.80G>T
ENST00000599899.5:n.1444G>T
ENST00000601008.1:c.242-1510G>T	ENSP00000471384.1:n.242-1510G>T
NM_000064.3:c.4485G>T	NP_000055.2:p.Pro1495=
NM_000064.4:c.4485G>T MANE Select	NP_000055.2:p.Pro1495=