Canonical Allele Identifier: CA2691480447

Gene: C5

Linked Data

• gnomAD v4: 9-120962782-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962782T>C , CM000671.2:g.120962782T>C	GRCh38
NC_000009.11:g.123725060T>C , CM000671.1:g.123725060T>C	GRCh37
NC_000009.10:g.122764881T>C	NCBI36
NG_007364.1:g.92495A>G , LRG_28:g.92495A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1433-6A>G
ENST00000696279.1:c.4719-6A>G
ENST00000696280.1:n.4488-6A>G
ENST00000696281.1:c.4417-6A>G	ENSP00000512521.1:n.4417-6A>G
ENST00000697921.1:n.3277-6A>G
ENST00000697922.1:c.*4389-6A>G	ENSP00000513478.1:n.*4389-6A>G
ENST00000697923.1:n.4844-6A>G
ENST00000223642.3:c.4399-6A>G MANE Select	ENSP00000223642.1:n.4399-6A>G
ENST00000223642.2:c.4399-6A>G	ENSP00000223642.1:n.4399-6A>G
NM_001735.2:c.4399-6A>G , LRG_28t1:c.4399-6A>G	NP_001726.2:n.4399-6A>G
XM_011518980.1:c.4414-6A>G	XP_011517282.1:n.4414-6A>G
NM_001317163.1:c.4417-6A>G	NP_001304092.1:n.4417-6A>G
NM_001317163.2:c.4417-6A>G	NP_001304092.1:n.4417-6A>G
NM_001735.3:c.4399-6A>G MANE Select	NP_001726.2:n.4399-6A>G