Canonical Allele Identifier: CA466940837

Gene: C5

Linked Data

• MyVariant Identifiers: chr9:g.123724995C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962717C>G , CM000671.2:g.120962717C>G	GRCh38
NC_000009.11:g.123724995C>G , CM000671.1:g.123724995C>G	GRCh37
NC_000009.10:g.122764816C>G	NCBI36
NG_007364.1:g.92560G>C , LRG_28:g.92560G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1492G>C
ENST00000696279.1:c.4778G>C
ENST00000696280.1:n.4547G>C
ENST00000696281.1:c.4476G>C	ENSP00000512521.1:p.Gly1492=
ENST00000697921.1:n.3336G>C
ENST00000697922.1:c.*4448G>C	ENSP00000513478.1:n.*4448G>C
ENST00000697923.1:n.4903G>C
ENST00000223642.3:c.4458G>C MANE Select	ENSP00000223642.1:p.Gly1486=
ENST00000223642.2:c.4458G>C	ENSP00000223642.1:p.Gly1486=
NM_001735.2:c.4458G>C , LRG_28t1:c.4458G>C	NP_001726.2:p.Gly1486=
XM_011518980.1:c.4473G>C	XP_011517282.1:p.Gly1491=
NM_001317163.1:c.4476G>C	NP_001304092.1:p.Gly1492=
NM_001317163.2:c.4476G>C	NP_001304092.1:p.Gly1492=
NM_001735.3:c.4458G>C MANE Select	NP_001726.2:p.Gly1486=