Canonical Allele Identifier: CA12970184
Gene: C5 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1035029

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.120980540G>A , CM000671.2:g.120980540G>A GRCh38
NC_000009.11:g.123742818G>A , CM000671.1:g.123742818G>A GRCh37
NC_000009.10:g.122782639G>A NCBI36
NG_007364.1:g.74737C>T , LRG_28:g.74737C>T

Transcript Alleles

HGVS Amino-acid change
NM_001735.2:c.3487-286C>T , LRG_28t1:c.3487-286C>T NP_001726.2:p.=
XM_011518980.1:c.3502-286C>T XP_011517282.1:p.=
NM_001317163.1:c.3505-286C>T VV NP_001304092.1:p.=
ENST00000223642.2:c.3487-286C>T ENSP00000223642.1:p.=
ENST00000489802.1:n.50-286C>T