HGVS | Genome Assembly |
---|---|
NC_000009.12:g.77794581A>C , CM000671.2:g.77794581A>C | GRCh38 |
NC_000009.11:g.80409497A>C , CM000671.1:g.80409497A>C | GRCh37 |
NC_000009.10:g.79599317A>C | NCBI36 |
NG_027904.2:g.241723T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000286548.9:c.617T>G MANE Select | ENSP00000286548.4:p.Val206Gly | |
ENST00000286548.8:c.617T>G | ENSP00000286548.4:p.Val206Gly | |
NM_002072.4:c.617T>G | NP_002063.2:p.Val206Gly | |
XM_017014628.2:c.443T>G | XP_016870117.1:p.Val148Gly | |
NM_002072.5:c.617T>G MANE Select | NP_002063.2:p.Val206Gly |