Canonical Allele Identifier: CA1762279561
Gene: MFHAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.8864738G= , CM000670.2:g.8864738G= GRCh38
NC_000008.10:g.8722248G= , CM000670.1:g.8722248G= GRCh37
NC_000008.9:g.8759658G= NCBI36
NG_009444.1:g.33884C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000276282.7:c.2998+25323C= MANE Select ENSP00000276282.6:n.2998+25323C=
ENST00000276282.6:c.2998+25323C= ENSP00000276282.6:n.2998+25323C=
NM_004225.2:c.2998+25323C= NP_004216.2:n.2998+25323C=
XR_246634.2:n.3534+25323C=
XM_024447330.1:c.2998+25323C= XP_024303098.1:n.2998+25323C=
NM_004225.3:c.2998+25323C= MANE Select NP_004216.2:n.2998+25323C=