Canonical Allele Identifier: CA466940884

Gene: C5

Linked Data

• MyVariant Identifiers: chr9:g.123725016T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962738T>G , CM000671.2:g.120962738T>G	GRCh38
NC_000009.11:g.123725016T>G , CM000671.1:g.123725016T>G	GRCh37
NC_000009.10:g.122764837T>G	NCBI36
NG_007364.1:g.92539A>C , LRG_28:g.92539A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1471A>C
ENST00000696279.1:c.4757A>C
ENST00000696280.1:n.4526A>C
ENST00000696281.1:c.4455A>C	ENSP00000512521.1:p.Ile1485=
ENST00000697921.1:n.3315A>C
ENST00000697922.1:c.*4427A>C	ENSP00000513478.1:n.*4427A>C
ENST00000697923.1:n.4882A>C
ENST00000223642.3:c.4437A>C MANE Select	ENSP00000223642.1:p.Ile1479=
ENST00000223642.2:c.4437A>C	ENSP00000223642.1:p.Ile1479=
NM_001735.2:c.4437A>C , LRG_28t1:c.4437A>C	NP_001726.2:p.Ile1479=
XM_011518980.1:c.4452A>C	XP_011517282.1:p.Ile1484=
NM_001317163.1:c.4455A>C	NP_001304092.1:p.Ile1485=
NM_001317163.2:c.4455A>C	NP_001304092.1:p.Ile1485=
NM_001735.3:c.4437A>C MANE Select	NP_001726.2:p.Ile1479=