HGVS | Genome Assembly |
---|---|
NC_000001.11:g.28863085C>T , CM000663.2:g.28863085C>T | GRCh38 |
NC_000001.10:g.29189597C>T , CM000663.1:g.29189597C>T | GRCh37 |
NC_000001.9:g.29062184C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000234961.7:c.921C>T MANE Select | ENSP00000234961.2:p.Gly307= | |
ENST00000234961.6:c.921C>T | ENSP00000234961.2:p.Gly307= | |
ENST00000621425.1:c.777C>T | ENSP00000477970.1:p.Gly259= | |
NM_000911.3:c.921C>T | NP_000902.3:p.Gly307= | |
NM_000911.4:c.921C>T MANE Select | NP_000902.3:p.Gly307= |