Canonical Allele Identifier: CA466941098

Gene: C5

Linked Data

• MyVariant Identifiers: chr9:g.123725195T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962917T>G , CM000671.2:g.120962917T>G	GRCh38
NC_000009.11:g.123725195T>G , CM000671.1:g.123725195T>G	GRCh37
NC_000009.10:g.122765016T>G	NCBI36
NG_007364.1:g.92360A>C , LRG_28:g.92360A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1408A>C
ENST00000696279.1:c.4694A>C
ENST00000696280.1:n.4463A>C
ENST00000696281.1:c.4392A>C	ENSP00000512521.1:p.Gly1464=
ENST00000697921.1:n.3252A>C
ENST00000697922.1:c.*4364A>C	ENSP00000513478.1:n.*4364A>C
ENST00000697923.1:n.4819A>C
ENST00000223642.3:c.4374A>C MANE Select	ENSP00000223642.1:p.Gly1458=
ENST00000223642.2:c.4374A>C	ENSP00000223642.1:p.Gly1458=
NM_001735.2:c.4374A>C , LRG_28t1:c.4374A>C	NP_001726.2:p.Gly1458=
XM_011518980.1:c.4389A>C	XP_011517282.1:p.Gly1463=
NM_001317163.1:c.4392A>C	NP_001304092.1:p.Gly1464=
NM_001317163.2:c.4392A>C	NP_001304092.1:p.Gly1464=
NM_001735.3:c.4374A>C MANE Select	NP_001726.2:p.Gly1458=