Canonical Allele Identifier: CA466940793

Gene: C5

Linked Data

• MyVariant Identifiers: chr9:g.123724977A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962699A>T , CM000671.2:g.120962699A>T	GRCh38
NC_000009.11:g.123724977A>T , CM000671.1:g.123724977A>T	GRCh37
NC_000009.10:g.122764798A>T	NCBI36
NG_007364.1:g.92578T>A , LRG_28:g.92578T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1510T>A
ENST00000696279.1:c.4796T>A
ENST00000696280.1:n.4565T>A
ENST00000696281.1:c.4494T>A	ENSP00000512521.1:p.Thr1498=
ENST00000697921.1:n.3354T>A
ENST00000697922.1:c.*4466T>A	ENSP00000513478.1:n.*4466T>A
ENST00000697923.1:n.4921T>A
ENST00000223642.3:c.4476T>A MANE Select	ENSP00000223642.1:p.Thr1492=
ENST00000223642.2:c.4476T>A	ENSP00000223642.1:p.Thr1492=
ENST00000480188.1:n.9T>A
NM_001735.2:c.4476T>A , LRG_28t1:c.4476T>A	NP_001726.2:p.Thr1492=
XM_011518980.1:c.4491T>A	XP_011517282.1:p.Thr1497=
NM_001317163.1:c.4494T>A	NP_001304092.1:p.Thr1498=
NM_001317163.2:c.4494T>A	NP_001304092.1:p.Thr1498=
NM_001735.3:c.4476T>A MANE Select	NP_001726.2:p.Thr1492=