Canonical Allele Identifier: CA374747826

Gene: C5

Linked Data

• gnomAD v4: 9-120962955-C-T
• MyVariant Identifiers: chr9:g.123725233C>T (hg19) ; chr9:g.120962955C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962955C>T , CM000671.2:g.120962955C>T	GRCh38
NC_000009.11:g.123725233C>T , CM000671.1:g.123725233C>T	GRCh37
NC_000009.10:g.122765054C>T	NCBI36
NG_007364.1:g.92322G>A , LRG_28:g.92322G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1370G>A
ENST00000696279.1:c.4656G>A
ENST00000696280.1:n.4425G>A
ENST00000696281.1:c.4354G>A	ENSP00000512521.1:p.Val1452Met
ENST00000697921.1:n.3214G>A
ENST00000697922.1:c.*4326G>A	ENSP00000513478.1:n.*4326G>A
ENST00000697923.1:n.4781G>A
ENST00000223642.3:c.4336G>A MANE Select	ENSP00000223642.1:p.Val1446Met
ENST00000223642.2:c.4336G>A	ENSP00000223642.1:p.Val1446Met
NM_001735.2:c.4336G>A , LRG_28t1:c.4336G>A	NP_001726.2:p.Val1446Met
XM_011518980.1:c.4351G>A	XP_011517282.1:p.Val1451Met
NM_001317163.1:c.4354G>A	NP_001304092.1:p.Val1452Met
NM_001317163.2:c.4354G>A	NP_001304092.1:p.Val1452Met
NM_001735.3:c.4336G>A MANE Select	NP_001726.2:p.Val1446Met