Canonical Allele Identifier: CA1876862584

Gene: C5

Linked Data

• dbSNP Id: rs2046770898

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120954528A>G , CM000671.2:g.120954528A>G	GRCh38
NC_000009.11:g.123716806A>G , CM000671.1:g.123716806A>G	GRCh37
NC_000009.10:g.122756627A>G	NCBI36
NG_007364.1:g.100749T>C , LRG_28:g.100749T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.4553T>C
ENST00000696279.1:c.5083-660T>C
ENST00000696280.1:n.4852-660T>C
ENST00000696281.1:c.4781-660T>C	ENSP00000512521.1:n.4781-660T>C
ENST00000697921.1:n.3641-660T>C
ENST00000697922.1:c.*4753-660T>C	ENSP00000513478.1:n.*4753-660T>C
ENST00000697923.1:n.7964T>C
ENST00000223642.3:c.4763-660T>C MANE Select	ENSP00000223642.1:n.4763-660T>C
ENST00000223642.2:c.4763-660T>C	ENSP00000223642.1:n.4763-660T>C
NM_001735.2:c.4763-660T>C , LRG_28t1:c.4763-660T>C	NP_001726.2:n.4763-660T>C
XM_011518980.1:c.4778-660T>C	XP_011517282.1:n.4778-660T>C
NM_001317163.1:c.4781-660T>C	NP_001304092.1:n.4781-660T>C
NM_001317163.2:c.4781-660T>C	NP_001304092.1:n.4781-660T>C
NM_001735.3:c.4763-660T>C MANE Select	NP_001726.2:n.4763-660T>C