HGVS | Genome Assembly |
---|---|
NC_000012.12:g.5045008G>T , CM000674.2:g.5045008G>T | GRCh38 |
NC_000012.11:g.5154174G>T , CM000674.1:g.5154174G>T | GRCh37 |
NC_000012.10:g.5024435G>T | NCBI36 |
NG_012198.1:g.6090G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252321.5:c.861G>T MANE Select | ENSP00000252321.3:p.Ala287= | |
ENST00000252321.4:c.861G>T | ENSP00000252321.3:p.Ala287= | |
NM_002234.3:c.861G>T | NP_002225.2:p.Ala287= | |
NM_002234.4:c.861G>T MANE Select | NP_002225.2:p.Ala287= |