Canonical Allele Identifier: CA199363955
Gene: C5 HGNC NCBI

Linked Data

dbSNP Id: rs907519944

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.120939684G>A , CM000671.2:g.120939684G>A GRCh38
NC_000009.11:g.123701962G>A , CM000671.1:g.123701962G>A GRCh37
NC_000009.10:g.122741783G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000696279.1:c.5899-5730C>T
ENST00000696280.1:n.5668-5730C>T
ENST00000696281.1:c.*548-5730C>T ENSP00000512521.1:n.*548-5730C>T
ENST00000697921.1:n.4457-5730C>T
ENST00000697922.1:c.*5569-5730C>T ENSP00000513478.1:n.*5569-5730C>T