Canonical Allele Identifier: CA859584644

Gene: C5

Linked Data

• dbSNP Id: rs1316547064
• gnomAD v3: 9-120980538-C-T
• gnomAD v4: 9-120980538-C-T
• MyVariant Identifiers: chr9:g.123742816C>T (hg19) ; chr9:g.120980538C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120980538C>T , CM000671.2:g.120980538C>T	GRCh38
NC_000009.11:g.123742816C>T , CM000671.1:g.123742816C>T	GRCh37
NC_000009.10:g.122782637C>T	NCBI36
NG_007364.1:g.74739G>A , LRG_28:g.74739G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.398-284G>A
ENST00000696279.1:c.3807-284G>A
ENST00000696280.1:n.3576-284G>A
ENST00000696281.1:c.3505-284G>A	ENSP00000512521.1:n.3505-284G>A
ENST00000697921.1:n.2365-284G>A
ENST00000697922.1:c.*3477-284G>A	ENSP00000513478.1:n.*3477-284G>A
ENST00000697923.1:n.3932-284G>A
ENST00000223642.3:c.3487-284G>A MANE Select	ENSP00000223642.1:n.3487-284G>A
ENST00000223642.2:c.3487-284G>A	ENSP00000223642.1:n.3487-284G>A
ENST00000489802.1:n.50-284G>A
NM_001735.2:c.3487-284G>A , LRG_28t1:c.3487-284G>A	NP_001726.2:n.3487-284G>A
XM_011518980.1:c.3502-284G>A	XP_011517282.1:n.3502-284G>A
NM_001317163.1:c.3505-284G>A	NP_001304092.1:n.3505-284G>A
NM_001317163.2:c.3505-284G>A	NP_001304092.1:n.3505-284G>A
NM_001735.3:c.3487-284G>A MANE Select	NP_001726.2:n.3487-284G>A