Canonical Allele Identifier: CA2747237283
Gene: CFHR5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196996012A>C , CM000663.2:g.196996012A>C GRCh38
NC_000001.10:g.196965142A>C , CM000663.1:g.196965142A>C GRCh37
NC_000001.9:g.195231765A>C NCBI36
NG_016365.1:g.23476A>C , LRG_227:g.23476A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000699466.1:c.536-10A>C ENSP00000514393.1:n.536-10A>C
ENST00000699467.1:n.860-10A>C
ENST00000699468.1:c.-24-102A>C ENSP00000514394.1:n.-24-102A>C
ENST00000256785.5:c.791-10A>C MANE Select ENSP00000256785.4:n.791-10A>C
ENST00000256785.4:c.791-10A>C ENSP00000256785.4:n.791-10A>C
NM_030787.3:c.791-10A>C , LRG_227t1:c.791-10A>C NP_110414.1:n.791-10A>C
XM_011510020.1:c.800-10A>C XP_011508322.1:n.800-10A>C
XM_011510020.2:c.800-10A>C XP_011508322.1:n.800-10A>C
NM_030787.4:c.791-10A>C MANE Select NP_110414.1:n.791-10A>C