Canonical Allele Identifier: CA1876858664

Gene: C5

Linked Data

• dbSNP Id: rs2046694677

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120938409C>T , CM000671.2:g.120938409C>T	GRCh38
NC_000009.11:g.123700687C>T , CM000671.1:g.123700687C>T	GRCh37
NC_000009.10:g.122740508C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000696279.1:c.5899-4455G>A
ENST00000696280.1:n.5668-4455G>A
ENST00000696281.1:c.*548-4455G>A	ENSP00000512521.1:n.*548-4455G>A
ENST00000697921.1:n.4457-4455G>A
ENST00000697922.1:c.*5569-4455G>A	ENSP00000513478.1:n.*5569-4455G>A