Canonical Allele Identifier: CA422802707

Gene: CFHR5

Linked Data

• dbSNP Id: rs1184721319
• gnomAD v2: 1-196964923-A-G
• MyVariant Identifiers: chr1:g.196964923A>G (hg19) ; chr1:g.196995793A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196995793A>G , CM000663.2:g.196995793A>G	GRCh38
NC_000001.10:g.196964923A>G , CM000663.1:g.196964923A>G	GRCh37
NC_000001.9:g.195231546A>G	NCBI36
NG_016365.1:g.23257A>G , LRG_227:g.23257A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699466.1:c.429A>G	ENSP00000514393.1:p.Gly143=
ENST00000699467.1:n.753A>G
ENST00000699468.1:c.-24-321A>G	ENSP00000514394.1:n.-24-321A>G
ENST00000256785.5:c.684A>G MANE Select	ENSP00000256785.4:p.Gly228=
ENST00000256785.4:c.684A>G	ENSP00000256785.4:p.Gly228=
NM_030787.3:c.684A>G , LRG_227t1:c.684A>G	NP_110414.1:p.Gly228=
XM_011510020.1:c.693A>G	XP_011508322.1:p.Gly231=
XM_011510020.2:c.693A>G	XP_011508322.1:p.Gly231=
NM_030787.4:c.684A>G MANE Select	NP_110414.1:p.Gly228=