Canonical Allele Identifier: CA13057857

Gene: C5

Linked Data

• dbSNP Id: rs2109897
• gnomAD v2: 9-123724508-A-G
• gnomAD v3: 9-120962230-A-G
• gnomAD v4: 9-120962230-A-G
• MyVariant Identifiers: chr9:g.123724508A>G (hg19) ; chr9:g.120962230A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962230A>G , CM000671.2:g.120962230A>G	GRCh38
NC_000009.11:g.123724508A>G , CM000671.1:g.123724508A>G	GRCh37
NC_000009.10:g.122764329A>G	NCBI36
NG_007364.1:g.93047T>C , LRG_28:g.93047T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1538+441T>C
ENST00000696279.1:c.4824+441T>C
ENST00000696280.1:n.4593+441T>C
ENST00000696281.1:c.4522+441T>C	ENSP00000512521.1:n.4522+441T>C
ENST00000697921.1:n.3382+441T>C
ENST00000697922.1:c.*4494+441T>C	ENSP00000513478.1:n.*4494+441T>C
ENST00000697923.1:n.4949+441T>C
ENST00000223642.3:c.4504+441T>C MANE Select	ENSP00000223642.1:n.4504+441T>C
ENST00000223642.2:c.4504+441T>C	ENSP00000223642.1:n.4504+441T>C
ENST00000480188.1:n.37+441T>C
NM_001735.2:c.4504+441T>C , LRG_28t1:c.4504+441T>C	NP_001726.2:n.4504+441T>C
XM_011518980.1:c.4519+441T>C	XP_011517282.1:n.4519+441T>C
NM_001317163.1:c.4522+441T>C	NP_001304092.1:n.4522+441T>C
NM_001317163.2:c.4522+441T>C	NP_001304092.1:n.4522+441T>C
NM_001735.3:c.4504+441T>C MANE Select	NP_001726.2:n.4504+441T>C