Canonical Allele Identifier: CA1876858679
Gene: C5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.120938435G= , CM000671.2:g.120938435G= GRCh38
NC_000009.11:g.123700713G= , CM000671.1:g.123700713G= GRCh37
NC_000009.10:g.122740534G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000696279.1:c.5899-4481C=
ENST00000696280.1:n.5668-4481C=
ENST00000696281.1:c.*548-4481C= ENSP00000512521.1:n.*548-4481C=
ENST00000697921.1:n.4457-4481C=
ENST00000697922.1:c.*5569-4481C= ENSP00000513478.1:n.*5569-4481C=