Canonical Allele Identifier: CA859584621

Gene: C5

Linked Data

• dbSNP Id: rs1390198712
• gnomAD v3: 9-120980430-A-T
• gnomAD v4: 9-120980430-A-T
• MyVariant Identifiers: chr9:g.123742708A>T (hg19) ; chr9:g.120980430A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.120980430A>T , CM000671.2:g.120980430A>T	GRCh38
NC_000009.11:g.123742708A>T , CM000671.1:g.123742708A>T	GRCh37
NC_000009.10:g.122782529A>T	NCBI36
NG_007364.1:g.74847T>A , LRG_28:g.74847T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000480188.2:n.398-176T>A
ENST00000696279.1:c.3807-176T>A
ENST00000696280.1:n.3576-176T>A
ENST00000696281.1:c.3505-176T>A	ENSP00000512521.1:n.3505-176T>A
ENST00000697921.1:n.2365-176T>A
ENST00000697922.1:c.*3477-176T>A	ENSP00000513478.1:n.*3477-176T>A
ENST00000697923.1:n.3932-176T>A
ENST00000223642.3:c.3487-176T>A MANE Select	ENSP00000223642.1:n.3487-176T>A
ENST00000223642.2:c.3487-176T>A	ENSP00000223642.1:n.3487-176T>A
ENST00000489802.1:n.50-176T>A
NM_001735.2:c.3487-176T>A , LRG_28t1:c.3487-176T>A	NP_001726.2:n.3487-176T>A
XM_011518980.1:c.3502-176T>A	XP_011517282.1:n.3502-176T>A
NM_001317163.1:c.3505-176T>A	NP_001304092.1:n.3505-176T>A
NM_001317163.2:c.3505-176T>A	NP_001304092.1:n.3505-176T>A
NM_001735.3:c.3487-176T>A MANE Select	NP_001726.2:n.3487-176T>A