Canonical Allele Identifier: CA1876862577

Gene: C5

Linked Data

• dbSNP Id: rs2046770773

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120954504C>T , CM000671.2:g.120954504C>T	GRCh38
NC_000009.11:g.123716782C>T , CM000671.1:g.123716782C>T	GRCh37
NC_000009.10:g.122756603C>T	NCBI36
NG_007364.1:g.100773G>A , LRG_28:g.100773G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000480188.2:n.4577G>A
ENST00000696279.1:c.5083-636G>A
ENST00000696280.1:n.4852-636G>A
ENST00000696281.1:c.4781-636G>A	ENSP00000512521.1:n.4781-636G>A
ENST00000697921.1:n.3641-636G>A
ENST00000697922.1:c.*4753-636G>A	ENSP00000513478.1:n.*4753-636G>A
ENST00000697923.1:n.7988G>A
ENST00000223642.3:c.4763-636G>A MANE Select	ENSP00000223642.1:n.4763-636G>A
ENST00000223642.2:c.4763-636G>A	ENSP00000223642.1:n.4763-636G>A
NM_001735.2:c.4763-636G>A , LRG_28t1:c.4763-636G>A	NP_001726.2:n.4763-636G>A
XM_011518980.1:c.4778-636G>A	XP_011517282.1:n.4778-636G>A
NM_001317163.1:c.4781-636G>A	NP_001304092.1:n.4781-636G>A
NM_001317163.2:c.4781-636G>A	NP_001304092.1:n.4781-636G>A
NM_001735.3:c.4763-636G>A MANE Select	NP_001726.2:n.4763-636G>A