Canonical Allele Identifier: CA1876859191
Gene: C5 HGNC NCBI

Linked Data

dbSNP Id: rs2046698619

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.120939724T>C , CM000671.2:g.120939724T>C GRCh38
NC_000009.11:g.123702002T>C , CM000671.1:g.123702002T>C GRCh37
NC_000009.10:g.122741823T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000696279.1:c.5899-5770A>G
ENST00000696280.1:n.5668-5770A>G
ENST00000696281.1:c.*548-5770A>G ENSP00000512521.1:n.*548-5770A>G
ENST00000697921.1:n.4457-5770A>G
ENST00000697922.1:c.*5569-5770A>G ENSP00000513478.1:n.*5569-5770A>G