Canonical Allele Identifier: CA466940896

Gene: C5

Linked Data

• MyVariant Identifiers: chr9:g.123725021G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962743G>T , CM000671.2:g.120962743G>T	GRCh38
NC_000009.11:g.123725021G>T , CM000671.1:g.123725021G>T	GRCh37
NC_000009.10:g.122764842G>T	NCBI36
NG_007364.1:g.92534C>A , LRG_28:g.92534C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1466C>A
ENST00000696279.1:c.4752C>A
ENST00000696280.1:n.4521C>A
ENST00000696281.1:c.4450C>A	ENSP00000512521.1:p.Arg1484=
ENST00000697921.1:n.3310C>A
ENST00000697922.1:c.*4422C>A	ENSP00000513478.1:n.*4422C>A
ENST00000697923.1:n.4877C>A
ENST00000223642.3:c.4432C>A MANE Select	ENSP00000223642.1:p.Arg1478=
ENST00000223642.2:c.4432C>A	ENSP00000223642.1:p.Arg1478=
NM_001735.2:c.4432C>A , LRG_28t1:c.4432C>A	NP_001726.2:p.Arg1478=
XM_011518980.1:c.4447C>A	XP_011517282.1:p.Arg1483=
NM_001317163.1:c.4450C>A	NP_001304092.1:p.Arg1484=
NM_001317163.2:c.4450C>A	NP_001304092.1:p.Arg1484=
NM_001735.3:c.4432C>A MANE Select	NP_001726.2:p.Arg1478=