Linked Data
ClinVar Variation Id:
700798
dbSNP Id:
rs150402693
gnomAD v2:
6-26093049-C-T
gnomAD v3:
6-26092821-C-T
gnomAD v4:
6-26092821-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.26092821C>T , CM000668.2:g.26092821C>T | GRCh38 |
| NC_000006.11:g.26093049C>T , CM000668.1:g.26093049C>T | GRCh37 |
| NC_000006.10:g.26201028C>T | NCBI36 |
| NG_008720.2:g.10541C>T , LRG_748:g.10541C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000485729.2:c.753C>T (HFE) | ENSP00000417534.2:p.Phe251= | |
| ENST00000707188.1:c.391-1787G>A (H2BC4) | ENSP00000516775.1:n.391-1787G>A | |
| ENST00000357618.10:c.753C>T (HFE) MANE Select | ENSP00000417404.1:p.Phe251= | |
| ENST00000309234.10:c.753C>T (HFE) | ENSP00000311698.6:p.Phe251= | |
| ENST00000317896.11:c.477C>T (HFE) | ENSP00000313776.7:p.Phe159= | |
| ENST00000336625.12:c.435C>T (HFE) | ENSP00000337819.8:p.Phe145= | |
| ENST00000349999.8:c.489C>T (HFE) | ENSP00000259699.6:p.Phe163= | |
| ENST00000352392.8:c.77-298C>T (HFE) | ENSP00000315936.4:n.77-298C>T | |
| ENST00000353147.9:c.213C>T (HFE) | ENSP00000312342.5:p.Phe71= | |
| ENST00000357618.9:c.753C>T (HFE) | ENSP00000417404.1:p.Phe251= | |
| ENST00000397022.7:c.684C>T (HFE) | ENSP00000380217.3:p.Phe228= | |
| ENST00000461397.5:c.711C>T (HFE) | ENSP00000420802.1:p.Phe237= | |
| ENST00000470149.5:c.744C>T (HFE) | ENSP00000419725.1:p.Phe248= | |
| ENST00000483782.1:n.1084C>T (HFE) | ||
| ENST00000486147.1:n.596C>T (HFE) | ||
| ENST00000488199.5:c.447C>T (HFE) | ENSP00000420559.1:p.Phe149= | |
| ENST00000629531.1:c.132+30952G>A (H2BC3) | ENSP00000486472.1:n.132+30952G>A | |
| NM_000410.3:c.753C>T , LRG_748t1:c.753C>T (HFE) | NP_000401.1:p.Phe251= | |
| NM_001300749.1:c.753C>T (HFE) | NP_001287678.1:p.Phe251= | |
| NM_139003.2:c.435C>T (HFE) | NP_620572.1:p.Phe145= | |
| NM_139004.2:c.477C>T (HFE) | NP_620573.1:p.Phe159= | |
| NM_139006.2:c.711C>T (HFE) | NP_620575.1:p.Phe237= | |
| NM_139007.2:c.489C>T (HFE) | NP_620576.1:p.Phe163= | |
| NM_139008.2:c.447C>T (HFE) | NP_620577.1:p.Phe149= | |
| NM_139009.2:c.684C>T (HFE) | NP_620578.1:p.Phe228= | |
| NM_139010.2:c.213C>T (HFE) | NP_620579.1:p.Phe71= | |
| NM_139011.2:c.77-298C>T (HFE) | NP_620580.1:n.77-298C>T | |
| XM_011514543.1:c.753C>T (HFE) | XP_011512845.1:p.Phe251= | |
| XM_011514544.1:c.744C>T (HFE) | XP_011512846.1:p.Phe248= | |
| XR_241893.2:n.875C>T (HFE) | ||
| XM_011514543.3:c.753C>T (HFE) | XP_011512845.1:p.Phe251= | |
| XR_241893.4:n.847C>T (HFE) | ||
| NM_001300749.2:c.753C>T (HFE) | NP_001287678.1:p.Phe251= | |
| NM_139003.3:c.435C>T (HFE) | NP_620572.1:p.Phe145= | |
| NM_139004.3:c.477C>T (HFE) | NP_620573.1:p.Phe159= | |
| NM_139006.3:c.711C>T (HFE) | NP_620575.1:p.Phe237= | |
| NM_139007.3:c.489C>T (HFE) | NP_620576.1:p.Phe163= | |
| NM_139008.3:c.447C>T (HFE) | NP_620577.1:p.Phe149= | |
| NM_139009.3:c.684C>T (HFE) | NP_620578.1:p.Phe228= | |
| NM_139010.3:c.213C>T (HFE) | NP_620579.1:p.Phe71= | |
| NM_139011.3:c.77-298C>T (HFE) | NP_620580.1:n.77-298C>T | |
| NM_000410.4:c.753C>T (HFE) MANE Select | NP_000401.1:p.Phe251= | |
| NM_001384164.1:c.753C>T (HFE) | NP_001371093.1:p.Phe251= |