Canonical Allele Identifier: CA1876858665
Gene: C5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.120938415A= , CM000671.2:g.120938415A= GRCh38
NC_000009.11:g.123700693A= , CM000671.1:g.123700693A= GRCh37
NC_000009.10:g.122740514A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000696279.1:c.5899-4461T=
ENST00000696280.1:n.5668-4461T=
ENST00000696281.1:c.*548-4461T= ENSP00000512521.1:n.*548-4461T=
ENST00000697921.1:n.4457-4461T=
ENST00000697922.1:c.*5569-4461T= ENSP00000513478.1:n.*5569-4461T=