Canonical Allele Identifier: CA466940917

Gene: C5

Linked Data

• MyVariant Identifiers: chr9:g.123725028T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962750T>G , CM000671.2:g.120962750T>G	GRCh38
NC_000009.11:g.123725028T>G , CM000671.1:g.123725028T>G	GRCh37
NC_000009.10:g.122764849T>G	NCBI36
NG_007364.1:g.92527A>C , LRG_28:g.92527A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1459A>C
ENST00000696279.1:c.4745A>C
ENST00000696280.1:n.4514A>C
ENST00000696281.1:c.4443A>C	ENSP00000512521.1:p.Val1481=
ENST00000697921.1:n.3303A>C
ENST00000697922.1:c.*4415A>C	ENSP00000513478.1:n.*4415A>C
ENST00000697923.1:n.4870A>C
ENST00000223642.3:c.4425A>C MANE Select	ENSP00000223642.1:p.Val1475=
ENST00000223642.2:c.4425A>C	ENSP00000223642.1:p.Val1475=
NM_001735.2:c.4425A>C , LRG_28t1:c.4425A>C	NP_001726.2:p.Val1475=
XM_011518980.1:c.4440A>C	XP_011517282.1:p.Val1480=
NM_001317163.1:c.4443A>C	NP_001304092.1:p.Val1481=
NM_001317163.2:c.4443A>C	NP_001304092.1:p.Val1481=
NM_001735.3:c.4425A>C MANE Select	NP_001726.2:p.Val1475=