Canonical Allele Identifier: CA466940768

Gene: C5

Linked Data

• dbSNP Id: rs1239906496
• gnomAD v2: 9-123724968-C-T
• gnomAD v4: 9-120962690-C-T
• MyVariant Identifiers: chr9:g.123724968C>T (hg19) ; chr9:g.120962690C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120962690C>T , CM000671.2:g.120962690C>T	GRCh38
NC_000009.11:g.123724968C>T , CM000671.1:g.123724968C>T	GRCh37
NC_000009.10:g.122764789C>T	NCBI36
NG_007364.1:g.92587G>A , LRG_28:g.92587G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480188.2:n.1519G>A
ENST00000696279.1:c.4805G>A
ENST00000696280.1:n.4574G>A
ENST00000696281.1:c.4503G>A	ENSP00000512521.1:p.Val1501=
ENST00000697921.1:n.3363G>A
ENST00000697922.1:c.*4475G>A	ENSP00000513478.1:n.*4475G>A
ENST00000697923.1:n.4930G>A
ENST00000223642.3:c.4485G>A MANE Select	ENSP00000223642.1:p.Val1495=
ENST00000223642.2:c.4485G>A	ENSP00000223642.1:p.Val1495=
ENST00000480188.1:n.18G>A
NM_001735.2:c.4485G>A , LRG_28t1:c.4485G>A	NP_001726.2:p.Val1495=
XM_011518980.1:c.4500G>A	XP_011517282.1:p.Val1500=
NM_001317163.1:c.4503G>A	NP_001304092.1:p.Val1501=
NM_001317163.2:c.4503G>A	NP_001304092.1:p.Val1501=
NM_001735.3:c.4485G>A MANE Select	NP_001726.2:p.Val1495=