Canonical Allele Identifier: CA1762279602
Gene: MFHAS1 HGNC NCBI

Linked Data

dbSNP Id: rs1808795781
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.8864803G>T , CM000670.2:g.8864803G>T GRCh38
NC_000008.10:g.8722313G>T , CM000670.1:g.8722313G>T GRCh37
NC_000008.9:g.8759723G>T NCBI36
NG_009444.1:g.33819C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000276282.7:c.2998+25258C>A MANE Select ENSP00000276282.6:n.2998+25258C>A
ENST00000276282.6:c.2998+25258C>A ENSP00000276282.6:n.2998+25258C>A
NM_004225.2:c.2998+25258C>A NP_004216.2:n.2998+25258C>A
XR_246634.2:n.3534+25258C>A
XM_024447330.1:c.2998+25258C>A XP_024303098.1:n.2998+25258C>A
NM_004225.3:c.2998+25258C>A MANE Select NP_004216.2:n.2998+25258C>A
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