Canonical Allele Identifier: CA199363266
Gene: C5 HGNC NCBI

Linked Data

dbSNP Id: rs75929624
MyVariant Identifiers: chr9:g.123700700T>C (hg19) chr9:g.120938422T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.120938422T>C , CM000671.2:g.120938422T>C GRCh38
NC_000009.11:g.123700700T>C , CM000671.1:g.123700700T>C GRCh37
NC_000009.10:g.122740521T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000696279.1:c.5899-4468A>G
ENST00000696280.1:n.5668-4468A>G
ENST00000696281.1:c.*548-4468A>G ENSP00000512521.1:n.*548-4468A>G
ENST00000697921.1:n.4457-4468A>G
ENST00000697922.1:c.*5569-4468A>G ENSP00000513478.1:n.*5569-4468A>G
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