Canonical Allele Identifier: CA5217183
Gene: C5 HGNC NCBI

Linked Data

dbSNP Id: rs779701089

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.120962824T>C , CM000671.2:g.120962824T>C GRCh38
NC_000009.11:g.123725102T>C , CM000671.1:g.123725102T>C GRCh37
NC_000009.10:g.122764923T>C NCBI36
NG_007364.1:g.92453A>G , LRG_28:g.92453A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000480188.2:n.1433-48A>G
ENST00000696279.1:c.4719-48A>G
ENST00000696280.1:n.4488-48A>G
ENST00000696281.1:c.4417-48A>G ENSP00000512521.1:n.4417-48A>G
ENST00000697921.1:n.3277-48A>G
ENST00000697922.1:c.*4389-48A>G ENSP00000513478.1:n.*4389-48A>G
ENST00000697923.1:n.4844-48A>G
ENST00000223642.3:c.4399-48A>G MANE Select ENSP00000223642.1:n.4399-48A>G
ENST00000223642.2:c.4399-48A>G ENSP00000223642.1:n.4399-48A>G
NM_001735.2:c.4399-48A>G , LRG_28t1:c.4399-48A>G NP_001726.2:n.4399-48A>G
XM_011518980.1:c.4414-48A>G XP_011517282.1:n.4414-48A>G
NM_001317163.1:c.4417-48A>G NP_001304092.1:n.4417-48A>G
NM_001317163.2:c.4417-48A>G NP_001304092.1:n.4417-48A>G
NM_001735.3:c.4399-48A>G MANE Select NP_001726.2:n.4399-48A>G