HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52488072T>C , CM000674.2:g.52488072T>C | GRCh38 |
NC_000012.11:g.52881856T>C , CM000674.1:g.52881856T>C | GRCh37 |
NC_000012.10:g.51168123T>C | NCBI36 |
NG_008298.1:g.10326A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000330722.7:c.1456A>G MANE Select | ENSP00000369317.3:p.Ile486Val | |
ENST00000330722.6:c.1456A>G | ENSP00000369317.3:p.Ile486Val | |
NM_005554.3:c.1456A>G | NP_005545.1:p.Ile486Val | |
NM_005554.4:c.1456A>G MANE Select | NP_005545.1:p.Ile486Val |