Canonical Allele Identifier: CA1128782939

Gene: C5

Linked Data

• dbSNP Id: rs2046983629
• gnomAD v3: 9-120980421-A-G
• gnomAD v4: 9-120980421-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120980421A>G , CM000671.2:g.120980421A>G	GRCh38
NC_000009.11:g.123742699A>G , CM000671.1:g.123742699A>G	GRCh37
NC_000009.10:g.122782520A>G	NCBI36
NG_007364.1:g.74856T>C , LRG_28:g.74856T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000480188.2:n.398-167T>C
ENST00000696279.1:c.3807-167T>C
ENST00000696280.1:n.3576-167T>C
ENST00000696281.1:c.3505-167T>C	ENSP00000512521.1:n.3505-167T>C
ENST00000697921.1:n.2365-167T>C
ENST00000697922.1:c.*3477-167T>C	ENSP00000513478.1:n.*3477-167T>C
ENST00000697923.1:n.3932-167T>C
ENST00000223642.3:c.3487-167T>C MANE Select	ENSP00000223642.1:n.3487-167T>C
ENST00000223642.2:c.3487-167T>C	ENSP00000223642.1:n.3487-167T>C
ENST00000489802.1:n.50-167T>C
NM_001735.2:c.3487-167T>C , LRG_28t1:c.3487-167T>C	NP_001726.2:n.3487-167T>C
XM_011518980.1:c.3502-167T>C	XP_011517282.1:n.3502-167T>C
NM_001317163.1:c.3505-167T>C	NP_001304092.1:n.3505-167T>C
NM_001317163.2:c.3505-167T>C	NP_001304092.1:n.3505-167T>C
NM_001735.3:c.3487-167T>C MANE Select	NP_001726.2:n.3487-167T>C