Canonical Allele Identifier: CA1876874375
Gene: C5 HGNC NCBI

Linked Data

dbSNP Id: rs2046984007

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.120980479T>C , CM000671.2:g.120980479T>C GRCh38
NC_000009.11:g.123742757T>C , CM000671.1:g.123742757T>C GRCh37
NC_000009.10:g.122782578T>C NCBI36
NG_007364.1:g.74798A>G , LRG_28:g.74798A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000480188.2:n.398-225A>G
ENST00000696279.1:c.3807-225A>G
ENST00000696280.1:n.3576-225A>G
ENST00000696281.1:c.3505-225A>G ENSP00000512521.1:n.3505-225A>G
ENST00000697921.1:n.2365-225A>G
ENST00000697922.1:c.*3477-225A>G ENSP00000513478.1:n.*3477-225A>G
ENST00000697923.1:n.3932-225A>G
ENST00000223642.3:c.3487-225A>G MANE Select ENSP00000223642.1:n.3487-225A>G
ENST00000223642.2:c.3487-225A>G ENSP00000223642.1:n.3487-225A>G
ENST00000489802.1:n.50-225A>G
NM_001735.2:c.3487-225A>G , LRG_28t1:c.3487-225A>G NP_001726.2:n.3487-225A>G
XM_011518980.1:c.3502-225A>G XP_011517282.1:n.3502-225A>G
NM_001317163.1:c.3505-225A>G NP_001304092.1:n.3505-225A>G
NM_001317163.2:c.3505-225A>G NP_001304092.1:n.3505-225A>G
NM_001735.3:c.3487-225A>G MANE Select NP_001726.2:n.3487-225A>G