Canonical Allele Identifier: CA1876865771
Gene: C5 HGNC NCBI

Linked Data

dbSNP Id: rs2046835144

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.120962594A>G , CM000671.2:g.120962594A>G GRCh38
NC_000009.11:g.123724872A>G , CM000671.1:g.123724872A>G GRCh37
NC_000009.10:g.122764693A>G NCBI36
NG_007364.1:g.92683T>C , LRG_28:g.92683T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000480188.2:n.1538+77T>C
ENST00000696279.1:c.4824+77T>C
ENST00000696280.1:n.4593+77T>C
ENST00000696281.1:c.4522+77T>C ENSP00000512521.1:n.4522+77T>C
ENST00000697921.1:n.3382+77T>C
ENST00000697922.1:c.*4494+77T>C ENSP00000513478.1:n.*4494+77T>C
ENST00000697923.1:n.4949+77T>C
ENST00000223642.3:c.4504+77T>C MANE Select ENSP00000223642.1:n.4504+77T>C
ENST00000223642.2:c.4504+77T>C ENSP00000223642.1:n.4504+77T>C
ENST00000480188.1:n.37+77T>C
NM_001735.2:c.4504+77T>C , LRG_28t1:c.4504+77T>C NP_001726.2:n.4504+77T>C
XM_011518980.1:c.4519+77T>C XP_011517282.1:n.4519+77T>C
NM_001317163.1:c.4522+77T>C NP_001304092.1:n.4522+77T>C
NM_001317163.2:c.4522+77T>C NP_001304092.1:n.4522+77T>C
NM_001735.3:c.4504+77T>C MANE Select NP_001726.2:n.4504+77T>C