Canonical Allele Identifier: CA466941164

Gene: C5

Linked Data

• MyVariant Identifiers: chr9:g.123725216A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962938A>G , CM000671.2:g.120962938A>G	GRCh38
NC_000009.11:g.123725216A>G , CM000671.1:g.123725216A>G	GRCh37
NC_000009.10:g.122765037A>G	NCBI36
NG_007364.1:g.92339T>C , LRG_28:g.92339T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1387T>C
ENST00000696279.1:c.4673T>C
ENST00000696280.1:n.4442T>C
ENST00000696281.1:c.4371T>C	ENSP00000512521.1:p.Thr1457=
ENST00000697921.1:n.3231T>C
ENST00000697922.1:c.*4343T>C	ENSP00000513478.1:n.*4343T>C
ENST00000697923.1:n.4798T>C
ENST00000223642.3:c.4353T>C MANE Select	ENSP00000223642.1:p.Thr1451=
ENST00000223642.2:c.4353T>C	ENSP00000223642.1:p.Thr1451=
NM_001735.2:c.4353T>C , LRG_28t1:c.4353T>C	NP_001726.2:p.Thr1451=
XM_011518980.1:c.4368T>C	XP_011517282.1:p.Thr1456=
NM_001317163.1:c.4371T>C	NP_001304092.1:p.Thr1457=
NM_001317163.2:c.4371T>C	NP_001304092.1:p.Thr1457=
NM_001735.3:c.4353T>C MANE Select	NP_001726.2:p.Thr1451=