Canonical Allele Identifier: CA1307828
Gene: CFHR5 HGNC NCBI

Linked Data

dbSNP Id: rs768102677

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196995758G>A , CM000663.2:g.196995758G>A GRCh38
NC_000001.10:g.196964888G>A , CM000663.1:g.196964888G>A GRCh37
NC_000001.9:g.195231511G>A NCBI36
NG_016365.1:g.23222G>A , LRG_227:g.23222G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000699466.1:c.394G>A ENSP00000514393.1:p.Gly132Ser
ENST00000699467.1:n.718G>A
ENST00000699468.1:c.-24-356G>A ENSP00000514394.1:n.-24-356G>A
ENST00000256785.5:c.649G>A MANE Select ENSP00000256785.4:p.Gly217Ser
ENST00000256785.4:c.649G>A ENSP00000256785.4:p.Gly217Ser
NM_030787.3:c.649G>A , LRG_227t1:c.649G>A NP_110414.1:p.Gly217Ser
XM_011510020.1:c.658G>A XP_011508322.1:p.Gly220Ser
XM_011510020.2:c.658G>A XP_011508322.1:p.Gly220Ser
NM_030787.4:c.649G>A MANE Select NP_110414.1:p.Gly217Ser