Canonical Allele Identifier: CA1876858668
Gene: C5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.120938423C= , CM000671.2:g.120938423C= GRCh38
NC_000009.11:g.123700701C= , CM000671.1:g.123700701C= GRCh37
NC_000009.10:g.122740522C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000696279.1:c.5899-4469G=
ENST00000696280.1:n.5668-4469G=
ENST00000696281.1:c.*548-4469G= ENSP00000512521.1:n.*548-4469G=
ENST00000697921.1:n.4457-4469G=
ENST00000697922.1:c.*5569-4469G= ENSP00000513478.1:n.*5569-4469G=