Canonical Allele Identifier: CA1876859161
Gene: C5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.120939660A= , CM000671.2:g.120939660A= GRCh38
NC_000009.11:g.123701938A= , CM000671.1:g.123701938A= GRCh37
NC_000009.10:g.122741759A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000696279.1:c.5899-5706T=
ENST00000696280.1:n.5668-5706T=
ENST00000696281.1:c.*548-5706T= ENSP00000512521.1:n.*548-5706T=
ENST00000697921.1:n.4457-5706T=
ENST00000697922.1:c.*5569-5706T= ENSP00000513478.1:n.*5569-5706T=