Canonical Allele Identifier: CA859587846
Gene: C5 HGNC NCBI

Linked Data

dbSNP Id: rs1328600106

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.120939751C>T , CM000671.2:g.120939751C>T GRCh38
NC_000009.11:g.123702029C>T , CM000671.1:g.123702029C>T GRCh37
NC_000009.10:g.122741850C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000696279.1:c.5899-5797G>A
ENST00000696280.1:n.5668-5797G>A
ENST00000696281.1:c.*548-5797G>A ENSP00000512521.1:n.*548-5797G>A
ENST00000697921.1:n.4457-5797G>A
ENST00000697922.1:c.*5569-5797G>A ENSP00000513478.1:n.*5569-5797G>A