Canonical Allele Identifier: CA1217885128

Gene: CFHR5

Linked Data

• dbSNP Id: rs1653980035

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.196995967T>A , CM000663.2:g.196995967T>A	GRCh38
NC_000001.10:g.196965097T>A , CM000663.1:g.196965097T>A	GRCh37
NC_000001.9:g.195231720T>A	NCBI36
NG_016365.1:g.23431T>A , LRG_227:g.23431T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699466.1:c.536-55T>A	ENSP00000514393.1:n.536-55T>A
ENST00000699467.1:n.860-55T>A
ENST00000699468.1:c.-24-147T>A	ENSP00000514394.1:n.-24-147T>A
ENST00000256785.5:c.791-55T>A MANE Select	ENSP00000256785.4:n.791-55T>A
ENST00000256785.4:c.791-55T>A	ENSP00000256785.4:n.791-55T>A
NM_030787.3:c.791-55T>A , LRG_227t1:c.791-55T>A	NP_110414.1:n.791-55T>A
XM_011510020.1:c.800-55T>A	XP_011508322.1:n.800-55T>A
XM_011510020.2:c.800-55T>A	XP_011508322.1:n.800-55T>A
NM_030787.4:c.791-55T>A MANE Select	NP_110414.1:n.791-55T>A