Canonical Allele Identifier: CA1762279592
Gene: MFHAS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.8864790A= , CM000670.2:g.8864790A= GRCh38
NC_000008.10:g.8722300A= , CM000670.1:g.8722300A= GRCh37
NC_000008.9:g.8759710A= NCBI36
NG_009444.1:g.33832T=

Transcript Alleles

HGVS Amino-acid change
ENST00000276282.7:c.2998+25271T= MANE Select ENSP00000276282.6:n.2998+25271T=
ENST00000276282.6:c.2998+25271T= ENSP00000276282.6:n.2998+25271T=
NM_004225.2:c.2998+25271T= NP_004216.2:n.2998+25271T=
XR_246634.2:n.3534+25271T=
XM_024447330.1:c.2998+25271T= XP_024303098.1:n.2998+25271T=
NM_004225.3:c.2998+25271T= MANE Select NP_004216.2:n.2998+25271T=