Canonical Allele Identifier: CA1876868351

Gene: C5

Linked Data

• dbSNP Id: rs1588168859

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120969024T>C , CM000671.2:g.120969024T>C	GRCh38
NC_000009.11:g.123731302T>C , CM000671.1:g.123731302T>C	GRCh37
NC_000009.10:g.122771123T>C	NCBI36
NG_007364.1:g.86253A>G , LRG_28:g.86253A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1254+37A>G
ENST00000696279.1:c.4540+37A>G
ENST00000696280.1:n.4309+37A>G
ENST00000696281.1:c.4238+37A>G	ENSP00000512521.1:n.4238+37A>G
ENST00000697921.1:n.3098+37A>G
ENST00000697922.1:c.*4210+37A>G	ENSP00000513478.1:n.*4210+37A>G
ENST00000697923.1:n.4665+37A>G
ENST00000223642.3:c.4220+37A>G MANE Select	ENSP00000223642.1:n.4220+37A>G
ENST00000223642.2:c.4220+37A>G	ENSP00000223642.1:n.4220+37A>G
NM_001735.2:c.4220+37A>G , LRG_28t1:c.4220+37A>G	NP_001726.2:n.4220+37A>G
XM_011518980.1:c.4235+37A>G	XP_011517282.1:n.4235+37A>G
NM_001317163.1:c.4238+37A>G	NP_001304092.1:n.4238+37A>G
NM_001317163.2:c.4238+37A>G	NP_001304092.1:n.4238+37A>G
NM_001735.3:c.4220+37A>G MANE Select	NP_001726.2:n.4220+37A>G