Canonical Allele Identifier: CA466941203

Gene: C5

Linked Data

• MyVariant Identifiers: chr9:g.123725231C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962953C>T , CM000671.2:g.120962953C>T	GRCh38
NC_000009.11:g.123725231C>T , CM000671.1:g.123725231C>T	GRCh37
NC_000009.10:g.122765052C>T	NCBI36
NG_007364.1:g.92324G>A , LRG_28:g.92324G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1372G>A
ENST00000696279.1:c.4658G>A
ENST00000696280.1:n.4427G>A
ENST00000696281.1:c.4356G>A	ENSP00000512521.1:p.Val1452=
ENST00000697921.1:n.3216G>A
ENST00000697922.1:c.*4328G>A	ENSP00000513478.1:n.*4328G>A
ENST00000697923.1:n.4783G>A
ENST00000223642.3:c.4338G>A MANE Select	ENSP00000223642.1:p.Val1446=
ENST00000223642.2:c.4338G>A	ENSP00000223642.1:p.Val1446=
NM_001735.2:c.4338G>A , LRG_28t1:c.4338G>A	NP_001726.2:p.Val1446=
XM_011518980.1:c.4353G>A	XP_011517282.1:p.Val1451=
NM_001317163.1:c.4356G>A	NP_001304092.1:p.Val1452=
NM_001317163.2:c.4356G>A	NP_001304092.1:p.Val1452=
NM_001735.3:c.4338G>A MANE Select	NP_001726.2:p.Val1446=