Canonical Allele Identifier: CA422663819
Gene: CFH HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.196716395A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.196747265A>T , CM000663.2:g.196747265A>T GRCh38
NC_000001.10:g.196716395A>T , CM000663.1:g.196716395A>T GRCh37
NC_000001.9:g.194983018A>T NCBI36
NG_007259.1:g.100255A>T , LRG_47:g.100255A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000367429.8:c.3648A>T ENSP00000356399.4:p.Thr1216=
NM_000186.3:c.3648A>T , LRG_47t1:c.3648A>T NP_000177.2:p.Thr1216=
NM_000186.4:c.3648A>T MANE Select NP_000177.2:p.Thr1216=