Canonical Allele Identifier: CA1762279628
Gene: MFHAS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.8864839T= , CM000670.2:g.8864839T= GRCh38
NC_000008.10:g.8722349T= , CM000670.1:g.8722349T= GRCh37
NC_000008.9:g.8759759T= NCBI36
NG_009444.1:g.33783A=

Transcript Alleles

HGVS Amino-acid change
ENST00000276282.7:c.2998+25222A= MANE Select ENSP00000276282.6:n.2998+25222A=
ENST00000276282.6:c.2998+25222A= ENSP00000276282.6:n.2998+25222A=
NM_004225.2:c.2998+25222A= NP_004216.2:n.2998+25222A=
XR_246634.2:n.3534+25222A=
XM_024447330.1:c.2998+25222A= XP_024303098.1:n.2998+25222A=
NM_004225.3:c.2998+25222A= MANE Select NP_004216.2:n.2998+25222A=
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