Canonical Allele Identifier: CA1876858685
Gene: C5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.120938445T= , CM000671.2:g.120938445T= GRCh38
NC_000009.11:g.123700723T= , CM000671.1:g.123700723T= GRCh37
NC_000009.10:g.122740544T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000696279.1:c.5899-4491A=
ENST00000696280.1:n.5668-4491A=
ENST00000696281.1:c.*548-4491A= ENSP00000512521.1:n.*548-4491A=
ENST00000697921.1:n.4457-4491A=
ENST00000697922.1:c.*5569-4491A= ENSP00000513478.1:n.*5569-4491A=