Canonical Allele Identifier: CA1128786348

Gene: C5

Linked Data

• dbSNP Id: rs2046833198
• gnomAD v3: 9-120962285-G-A
• gnomAD v4: 9-120962285-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962285G>A , CM000671.2:g.120962285G>A	GRCh38
NC_000009.11:g.123724563G>A , CM000671.1:g.123724563G>A	GRCh37
NC_000009.10:g.122764384G>A	NCBI36
NG_007364.1:g.92992C>T , LRG_28:g.92992C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1538+386C>T
ENST00000696279.1:c.4824+386C>T
ENST00000696280.1:n.4593+386C>T
ENST00000696281.1:c.4522+386C>T	ENSP00000512521.1:n.4522+386C>T
ENST00000697921.1:n.3382+386C>T
ENST00000697922.1:c.*4494+386C>T	ENSP00000513478.1:n.*4494+386C>T
ENST00000697923.1:n.4949+386C>T
ENST00000223642.3:c.4504+386C>T MANE Select	ENSP00000223642.1:n.4504+386C>T
ENST00000223642.2:c.4504+386C>T	ENSP00000223642.1:n.4504+386C>T
ENST00000480188.1:n.37+386C>T
NM_001735.2:c.4504+386C>T , LRG_28t1:c.4504+386C>T	NP_001726.2:n.4504+386C>T
XM_011518980.1:c.4519+386C>T	XP_011517282.1:n.4519+386C>T
NM_001317163.1:c.4522+386C>T	NP_001304092.1:n.4522+386C>T
NM_001317163.2:c.4522+386C>T	NP_001304092.1:n.4522+386C>T
NM_001735.3:c.4504+386C>T MANE Select	NP_001726.2:n.4504+386C>T